Disorders


 

Tuberous Sclerosis 2


Synonym(s): TSC2

 

OMIM

GeneLocusProtein
TSC216p13.3Tuberin

Laboratory Test Method Prenatal Carrier *
Addenbrooke's Hospital, Molecular Genetics Laboratory - Cambridge, Great Britain• Linkage analysis
  
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA  
bio.logis Center for Human Genetics - Frankfurt, Germany  
CeGaT GmbH - Tuebingen, Germany  
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
Cliniques universitaires Saint Luc, Center for Human Genetics - Brussels, Belgium  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
diagenos - Osnabrueck, Germany• Mutation scanning of the entire coding region
  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  
GGA - Galil Genetic Analysis - Kazerin, Israel  
Innovagenomics S.L, Innovagenomics - Salamanca, Spain  
Institute of Medical Genetics, All Wales Molecular Genetics Laboratory - Cardiff, Great Britain• Mutation scanning of the entire coding region
  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Medgene, MedGene - Bratislava, Slovakia  
Praxis fuer Humangenetik Wien - Vienna, Austria  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea  
Shafallah Medical Genetics Center, SMGC Laboratory - Doha, Qatar  
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain  

* 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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