Disorders


 

Crigler-Najjar Syndrome


 

OMIM

GeneLocusProtein
UGT1A12q37UDP-glucuronosyltransferase 1-1

Laboratory Test Method Prenatal Carrier *
bio.logis Center for Human Genetics - Frankfurt, Germany  
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany• Targeted mutation analysis
  
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  
Children's University Hospital, Human Genetics - Berne, Switzerland• Mutation scanning of the entire coding region
  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
diagenos - Osnabrueck, Germany  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany  
Innovagenomics S.L, Innovagenomics - Salamanca, Spain  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Mayo Clinic, Nucleotide Polymorphism Lab - Rochester, MN, USA  
Medgene, MedGene - Bratislava, Slovakia  
Praxis fuer Humangenetik Wien - Vienna, Austria  
Sheffield Children's NHS Foundation Trust, Sheffield Diagnostic Genetics Service - Sheffield, Great Britain  
Sir Ganga Ram Hospital, Center of Medical Genetics - New Delhi, India  
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain  
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany  
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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