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SWITZERLAND

Suisse Romande
GENÈVE

Accreditation Search of duplications and/or deletions by array-CGH
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Deletion / Duplication analysis, Detection of chromosome alterations large in size
Technique(s) : Array based techniques, FISH

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SWITZERLAND

Suisse Romande
GENÈVE

Accreditation Aneuploïdy screening (chromosomes 13, 18, 21, X and Y): interphasic FISH or QF-PCR testing.
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Deletion / Duplication analysis, Detection of chromosome alterations large in size
Technique(s) : PCR based techniques, FISH

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SWITZERLAND

Suisse Alémanique
SCHLIEREN

Accreditation Aneuploïd screen (chromosomes 13, 18, 21, X and Y) by interphase FISH or QFPCR
Universität Zürich
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

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GERMANY

Bayern
MÜNCHEN

Accreditation FISH on interphase nuclei to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GERMANY

Schleswig-Holstein
LÜBECK

Accreditation FISH on interphase nuclei to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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NETHERLANDS

Limburg
MAASTRICHT

Accreditation Cytogenetic analysis and aneuploidy screen (chromosomes 13, 18, 21, X, Y)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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GERMANY

Thüringen
JENA

Accreditation Rapid FISH on interphase nuclei and STR prenatal rapid test to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Institut für Humangenetik am Universitätsklinikum Jena
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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SWITZERLAND

Suisse Alémanique
ZÜRICH

Accreditation Aneuploïd screen (chromosomes 13, 18, 21, X and Y): Interphase FISH and/or QF-PCR analysis
Genetica AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GERMANY

Thüringen
JENA

Accreditation Diagnosis of aneuploidia (all chromosomes)
Institut für Humangenetik am Universitätsklinikum Jena
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : M-FISH/SKY, Array based techniques, FISH, Karyotyping

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FRANCE

BOURGOGNE-FRANCHE-COMTE
BESANÇON

Accreditation Diagnosis of aneuploidy (interphase FISH of chromosomes 13, 18, 21, X and Y)
CHRU de Besançon - Hôpital Jean Minjoz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GERMANY

Bayern
MÜNCHEN

Accreditation Diagnosis of aneuploidy in chromosomes 13, 18, 21, X, Y
Zweigniederlassung der SYNLAB MVZ Augsburg GmbH
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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FRANCE

OUTRE-MER
SCHOELCHER

Accreditation Diagnosis of aneuploidies (by FISH: chromosomes 13, 18, 21, X and Y)
BIOLAB Martinique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

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NETHERLANDS

Gelderland
NIJMEGEN

Accreditation Molecular and cytogenetic diagnosis of Chromosomal Anomalies (Karyotyping, SNP-Array and FISH)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technique(s) : FISH

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UNITED KINGDOM

Merseyside
LIVERPOOL

Accreditation Molecular diagnosis of Sex Determination For X-Linked Conditions For Disorders That Manifest Significantly Different In One Sex Compared To The Other by Targetted Mutation and Copy Number Analysis (Genes: AMELX, AMELY, SRY)
Liverpool Women's NHS Foundation Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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GERMANY

Nordrhein-Westfalen
AACHEN

Accreditation Cytogenetic lab for conventional and molecular cytogenetic chromosome analysis
Universitätsklinikum Aachen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

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GERMANY

Schleswig-Holstein
KIEL

Accreditation Cytogenetic lab for prenatal and postnatal chromosome analysis
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation Diagnosis of microdeletion / microduplication syndromes
Hôpital Saint-Joseph
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications

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UNITED KINGDOM

Greater Manchester
MANCHESTER

Accreditation Molecular diagnosis of aneuploidy (chromosomes 13, 18, 21, X and Y; by QF-PCR)
St Mary's Hospital
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation Diagnosis of chromosomal anomalies (Array CGH by DNA-SNP chips)
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Newborn screening
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : Array based techniques, FISH, Karyotyping

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SWITZERLAND

Suisse Romande
GENÈVE

Accreditation Non invasive prenatal testing of trisomy 13,18,21 and sex chromosomes (NIPT)
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Antenatal diagnosis, Risk assessment
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES)

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FRANCE

OCCITANIE
MONTPELLIER

Accreditation Chromosomal Microarray Analysis (CMA)
CHU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technique(s) : Array based techniques

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FRANCE

OCCITANIE
MONTPELLIER

Accreditation Diagnosis of chromosomal anomalies
CHU de Montpellier - Hôpital Arnaud de Villeneuve
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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BELGIUM

LIEGE
LIEGE

Accreditation Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 and 21 and sex chromosomes
Centre Hospitalier Régional de la Citadelle
Purpose(s) : Antenatal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : Array based techniques

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BELGIUM

OOST-VLAANDEREN
GENT

Accreditation Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 and 21 and sex chromosomes
Center for Medical Genetics Gent
Purpose(s) : Antenatal diagnosis, Risk assessment
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES)

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UNITED KINGDOM

Antrim and Newtownabbey
BELFAST

Accreditation Molecular diagnosis of Turner syndrome (Y-STS multiplex)
Belfast City Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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CANADA

Ontario
TORONTO

Accreditation Molecular Diagnosis of Aneuploidy (QF-PCR 13, 18, 21, X, Y)
North York General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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CANADA

Terre-Neuve-et-Labrador
ST. JOHN'S

Accreditation Rapid Aneuploidy Detection (qfPCR)
Health Sciences Centre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

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CANADA

Ontario
HAMILTON

Accreditation Rapid Aneuploidy Detection (QF-PCR 13/18/21/X/Y Analysis)
McMaster University Medical Centre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : PCR based techniques

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CANADA

Ontario
TORONTO

Accreditation Rapid Aneuploidy Detection (iFISH 13/18/21/X/Y probe analysis)
The Hospital for Sick Children
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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CANADA

Ontario
OTTAWA

Accreditation Prenatal Rapid Aneuploidy Detection (qfPCR)
Children's Hospital of Eastern Ontario
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : PCR based techniques

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CANADA

Ontario
OTTAWA

Accreditation Molecular Cytogenetic Diagnosis of Numerical Sex Chromosome Anomaly (FISH CEP XY probe analysis)
Children's Hospital of Eastern Ontario
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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CANADA

Ontario
TORONTO

Accreditation Rapid Aneuploidy Detection (Aneufast 13/18/21/X/Y probe QF-PCR)
North York General Hospital
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : PCR based techniques

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GREECE

ATTIKI
ATHENS

Aneuploidy screen by PCR (chromosomes 13, 18, 21, X, Y)
Diagnostic Genetic Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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SPAIN

Cataluña
BARCELONA

Diagnosis of chromosomal anomalies (SNP array)
Reprogenetics Spain S.A.
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Molecular genetics, Other
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing, PCR based techniques

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GREECE

ATTIKI
MAROUSI

Clinical laboratory for cytogenetic testing
Private clinic for subfertility studies
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

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ITALY

LAZIO
ROMA

Molecular genetic diagnosis of cryptic rearrangements by array-CGH
Istituto CSS-Mendel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : Array based techniques

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ITALY

LAZIO
ROMA

Molecular diagnosis of aneuploidy (chromosome 13, 18, 21, X and Y) determined by QF-PCR
Istituto CSS-Mendel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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ITALY

LAZIO
ROMA

Molecular genetic diagnosis of criptic rearrangements by array-CGH
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : Array based techniques

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ITALY

SICILIA
CATANIA

Molecular diagnosis of aneuploidy (chromosome 13, 18, 21, X and Y) determined by QF-PCR
CPSS - Centro Polidiagnostico Servizi Sanitari
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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FRANCE

GRAND-EST
STRASBOURG

Diagnosis of Robertsonian and reciprocal translocations, other chromosomal anomalies and X-linked diseases
Hôpitaux Universitaires de Strasbourg - HUS
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size

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ITALY

PIEMONTE
TORINO

Molecular genetic diagnosis of genomic microdeletions-duplications by CGH-array
A.O.U. Città della Salute e della Scienza di Torino - Ospedale Molinette
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Deletion / Duplication analysis, Detection of microdeletions/microduplications
Technique(s) : Array based techniques

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SPAIN

País Vasco
SAN SEBASTIÁN

Diagnosis of aneuploidy (QF-PCR technique, chromosomes 13, 18, 21, X and Y)
Hospital Universitario Donostia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Other

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POLAND

Warszawa
WARSZAWA

Cytogenetic diagnosis of constitutional chromosomal abnormalities (microdeletion/ microduplication syndromes by FISH, MLPA, array CGH: MLPA kits P245, P297, P036)
Instytut Matki i Dziecka
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : MLPA based techniques, Array based techniques, FISH, Karyotyping

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ITALY

LOMBARDIA
MILANO

Diagnosis of aneuploidies of 13, 18, 21, X, Y chromosomes
Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Deletion / Duplication analysis, Detection of chromosome alterations large in size
Technique(s) : PCR based techniques, FISH, Karyotyping

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SPAIN

Madrid
MADRID

Diagnosis of Turner syndrome
Hospital Universitario Fundación Jiménez Díaz
Purpose(s) : Antenatal diagnosis, Pre-implantation diagnosis, Post-natal diagnosis, Risk assessment
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : Array based techniques, Karyotyping

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SWITZERLAND

Suisse Alémanique
SCHLIEREN

Molecular cytogenetic diagnosis of Turner syndrome
Center for Cardiovascular Genetics and Gene Diagnostics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

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DENMARK

Sjælland
GLOSTRUP

Molecular and cytogenetic diagnosis of aneuploidies of chromosomes 13, 18, 21, X and Y (QF-PCR ; interphase FISH)
Kennedy Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

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POLAND

Warszawa
WARSZAWA

Molecular and cytogenetic diagnosis of trisomies (FISH, MLPA, array CGH: MLPA kit P095)
Instytut Matki i Dziecka
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : MLPA based techniques, FISH, Karyotyping

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SPAIN

Cataluña
BARCELONA

Diagnosis of Turner syndrome (PCR-based STR analysis)
Hospital Universitari Vall d'Hebron
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Other

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SPAIN

Comunidad Valenciana
SANT JOAN D'ALACANT

Prenatal molecular diagnosis of aneuploidy (chromosomes 13, 18, 21, X and Y / QF-PCR)
Centro Inmunológico de Alicante (CIALAB)
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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SPAIN

Comunidad Valenciana
ALICANTE

Diagnosis of aneuploidy (chromosomes 13, 18, 21, X and Y / detection of chromosome alterations large in size, PCR based techniques)
Hospital Clínica Vistahermosa
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Other

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ITALY

SICILIA
AVOLA

Diagnosis of aneuploidy - chromosomes 13, 18, 21, X
Laboratori Campisi s.r.l.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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ITALY

SICILIA
AVOLA

Diagnosis of Turner syndrome
Laboratori Campisi s.r.l.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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ITALY

VENETO
LIMENA

Molecular diagnosis of aneuploidy (analysis of 13, 18, 21, X and Y chromosomes determined by QF-PCR)
RDI - RETE DIAGNOSTICA ITALIANA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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POLAND

Gdansk
GDANSK

PGS-NGS 360°?. Preimplantation Genetic Screening
INVICTA Sp. z o.o.
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES)

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HUNGARY

Közép-Magyarország
DEBRECEN

Cytogenetic diagnosis of aneuploidies and structural rearrangements
University of Debrecen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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CANADA

Alberta
EDMONTON

Rapid Aneuploidy Detection (13/18/21/X/Y qfPCR analysis)
University of Alberta
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES), FISH

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ITALY

LAZIO
ROMA

Molecular cytogenetics diagnosis of aneuploidy (chromosome 13, 18, 21, X and Y)
ASLRM1 - Centro per la tutela della Salute della Donna e del Bambino
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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ITALY

LOMBARDIA
SAN FERMO DELLA BATTAGLIA

Cytogenetic diagnosis of Turner syndrome
ASST Lariana - Ospedale S.Anna di Como
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

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AUSTRIA

SALZBURG
SALZBURG

Search for genomic Y chromosome sequences in Turner syndrome (SRY)
Universitätsklinikum der Paracelsus Medizinischen Privatuniversität
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Other

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ITALY

EMILIA ROMAGNA
FERRARA

Diagnosis of chromosomal anomalies
A.O.U. Sant'Anna - Polo Chimico-Bio-Medico
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications, Chromosomal instability
Technique(s) : NGS sequencing (except WES), M-FISH/SKY, MLPA based techniques, Array based techniques, FISH, Karyotyping, Chromosome breakage analysis

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ITALY

PUGLIA
CARBONARA DI BARI

Molecular genetic diagnosis of cryptic intrachromosomal and subtelomeric rearrangement by array-CGH
Ospedale di Venere - ASL Bari
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : Array based techniques

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GERMANY

Hessen
BAD NAUHEIM

Rapid FISH on interphase nuclei to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Zweigniederlassung der SYNLAB MVZ Kassel GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GERMANY

Hessen
GIEßEN

FISH on interphase nuclei to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Humangenetische Praxis Dr. Schmidt & Mautner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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ROMANIA

IASI
IASI

Aneuploïd screen (chromosomes 13, 18, 21, X and Y) by interphase FISH
Spitalul clinic de obstetrica si ginecologie Cuza Voda
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

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ROMANIA

BUCURESTI
BUCURESTI

Aneuploïd screen (chromosomes 13, 18, 21, X and Y) by interphase FISH
Spitalul Judetean Ilfov
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

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SWITZERLAND

Suisse Alémanique
BASEL

Aneuploïd screen (chromosomes 13, 18, 21, X and Y) by interphase FISH
University Children's Hospital - UKBB
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GREECE

ATTIKI
ATHENS

Aneuploidy screen by PCR and MLPA (chromosomes 13, 18, 21, X, Y)
Mitera General, Maternity and Children's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques, MLPA based techniques

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ITALY

MARCHE
FANO

Molecular diagnosis of aneuploidy (chromosomes 13, 18, 21, X and Y)
Associazione Cante di Montevecchio
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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BULGARIA

 South-West region
SOFIA

Molecular diagnosis of aneuploidy (chromosomes 13, 18, 21, X and Y)
University hospital of Obstetrics and Gynecology
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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SLOVENIA

SLOVENIA
MARIBOR

Cytogenetic analyses of chromosomal anomalies
Maribor general hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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PORTUGAL

SUL
LISBOA

Search for genomic Y chromosome sequences in Turner syndrome patients
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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ROMANIA

BUCURESTI
BUCURESTI

Aneuploidy screen by FISH analysis (chromosomes 13, 18, 21, X, Y)
GeneticLab
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

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BULGARIA

 South Central region
PLOVDIV

Molecular cytogenetic diagnosis of Turner syndrome
University Hospital Plovdiv - UMHAT Sv. Georgi - EAD
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

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GERMANY

Rheinland-Pfalz
KAISERSLAUTERN

Rapid FISH on interphase nuclei to detect specific trisomies (numeric aberration of 13/18/21/X/Y)
Med-Biolog-Labor
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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GERMANY

Rheinland-Pfalz
KAISERSLAUTERN

Diagnosis of Turner syndrome
Med-Biolog-Labor
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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SERBIA

Serbia
BELGRADE

Prenatal and postnatal molecular cytogenetic diagnosis of chromosomal anomalies (by FISH)
Mother and Child Health Institute of Serbia "Dr Vukan Cupic"
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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CZECH REPUBLIC

Hradec Kralove
HRADEC KRALOVE

Molecular cytogenetic diagnosis of aneuploidy (FISH on chromosomes 13, 18, 21, X and Y)
Medical Genetics Laboratory
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

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ITALY

PIEMONTE
VERCELLI

Cytogenetic diagnosis of Turner syndrome
Ospedale S. Andrea - ASL VC
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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ITALY

CAMPANIA
NAPOLI

Molecular cytogenetics diagnosis of aneuploidy (chromosome 13, 18, 21, X and Y; FISH analysis)
Azienda Ospedaliera Universitaria "Federico II"
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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ITALY

UMBRIA
PERUGIA

Cytogenetic diagnosis of Turner syndrome
Genetics 2000 S.r.l.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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ITALY

VENETO
PADOVA

Personalised preimplantation genetic diagnosis: microsatellite analysis on the first polar globule
Policlinico Universitario di Padova
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Molecular genetics

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POLAND

Warszawa
WARSAW

Molecular diagnosis of aneuploidy syndromes (MLPA kit P095)
Instytut "Pomnik-Centrum Zdrowia Dziecka"
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : MLPA based techniques

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ITALY

PUGLIA
LECCE

Molecular diagnosis of aneuploidy - chromosomes 13, 18, 21, X and Y by FISH and QF-PCR
Presidio Ospedaliero "Vito Fazzi" - ASL LE
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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PORTUGAL

CENTRO
OEIRAS

Prenatal and postnatal molecular genetic diagnosis of Turner Syndrome (MLPA)
Laboratório de Análises Clínicas Dr. Joaquim Chaves
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : MLPA based techniques

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CANADA

Alberta
CALGARY

Prenatal Rapid Aneuploidy Detection (qfPCR)
Alberta Children's Hospital
Purpose(s) : Antenatal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : PCR based techniques

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CANADA

Alberta
CALGARY

Molecular Cytogenetic Diagnosis of Numerical Sex Chromosome Anomaly (i,mFISH CEP XY probe analysis)
Alberta Children's Hospital
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : M-FISH/SKY, FISH

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CANADA

Alberta
CALGARY

Rapid Aneuploidy Detection (iFISH 13/18/21/X/Y probe analysis)
Alberta Children's Hospital
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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ITALY

PUGLIA
GROTTAGLIE

Antenatal and postnatal molecular cytogenetic diagnosis of aneuploidy in chromosomes 13, 18, 21, X and Y (determined by FISH)
Presidio Ospedaliero Centrale - Ospedale "San Marco"
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

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ITALY

VENETO
PADOVA

Diagnosis of aneuploidy (analysis of 13, 18, 21, X and Y chromosomes) determined by CGH-array
Policlinico Universitario di Padova
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Deletion / Duplication analysis, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : PCR based techniques, Array based techniques, Karyotyping

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