Search for a diagnostic test
90 Result(s)
Caption
: Accreditation
= ;

Suisse Romande
GENÈVE
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

Suisse Romande
GENÈVE
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

Suisse Alémanique
SCHLIEREN
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

Bayern
MÜNCHEN
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

Schleswig-Holstein
LÜBECK
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

Limburg
MAASTRICHT
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

Thüringen
JENA
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

Suisse Alémanique
ZÜRICH
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

Thüringen
JENA
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

BOURGOGNE-FRANCHE-COMTE
BESANÇON
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

Bayern
MÜNCHEN
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

OUTRE-MER
SCHOELCHER
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

Gelderland
NIJMEGEN
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

Merseyside
LIVERPOOL
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

Nordrhein-Westfalen
AACHEN
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

Schleswig-Holstein
KIEL
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

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Diagnosis of microdeletion / microduplication syndromes
Hôpital Saint-Joseph
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Cytogenetics
Objective(s)
: Detection of microdeletions/microduplications

Greater Manchester
MANCHESTER
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

ILE-DE-FRANCE
PARIS
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

Suisse Romande
GENÈVE
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)

OCCITANIE
MONTPELLIER
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

OCCITANIE
MONTPELLIER
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

LIEGE
LIEGE
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

OOST-VLAANDEREN
GENT
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)

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

Ontario
TORONTO
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

Terre-Neuve-et-Labrador
ST. JOHN'S
Rapid Aneuploidy Detection (qfPCR)
Health Sciences Centre
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Cytogenetics

Ontario
HAMILTON
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

Ontario
TORONTO
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

Ontario
OTTAWA
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

Ontario
OTTAWA
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

Ontario
TORONTO
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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

VENETO
PADOVA