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                                                                  Laboratory officially designated for this diagnostic test =Laboratory officially designated for this diagnostic test            Accreditation =Accreditation ;

GERMANY

Baden-Württemberg
TÜBINGEN

Diagnosis of constitutional megaloblastic anemia with severe neurologic disease (DHFR gene)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
NETHERLANDS

Gelderland
NIJMEGEN

Molecular diagnosis of Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency (DHFR gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
NETHERLANDS

Noord-Holland
AMSTERDAM

Diagnosis of Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency (DHFR gene; Analytes: 5-Methyltetrahydrofolate en Pterines)
Amsterdam UMC, locatie AMC
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics, Biochemical genetics
Service(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Analyte / Enzyme assay sanger sequencing

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Accreditation
GERMANY

Baden-Württemberg
ULM

Diagnosis of constitutional megaloblastic anemia with severe neurologic disease (DHFR gene)
DRK Baden-Württemberg/ Hessen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Sequence analysis: entire coding region sanger sequencing

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Accreditation
SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of constitutional megaloblastic anemia with severe neurologic disease (DHFR gene)
LabGenetics - Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Service(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region sanger sequencing

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SPAIN

Madrid
CANTOBLANCO

Diagnosis of constitutional megaloblastic anemia with severe neurologic disease (DHFR gene)
Universidad Autónoma de Madrid. Facultad de Ciencias
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Newborn screening
Specialty(ies) : Molecular genetics, Biochemical genetics
Service(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Analyte / Enzyme assay ngs sequencing (except wes), sanger sequencing

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