Disorders


 

TGFBR1-Related Thoracic Aortic Aneurysms and Aortic Dissections


Synonym(s): TGFBR1-Related TAAD, TGFBR1-Related Thoracic Aortic Aneurysms and Dissection, TGFBR1-Related Thoracic Aortic Dissection

 

OMIM

GeneLocusProtein
TGFBR19q22TGF-beta receptor type-1

Laboratory Test Method Prenatal Carrier *
Baylor College of Medicine, John Welsh Cardiovascular Diagnostic Laboratory - Houston, TX, USA  
BC Children's and BC Women's Hospitals, Molecular Genetics Laboratory - Vancouver, Canada  
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany  
Center for Human Genetics Freiburg, Kohlhase Laboratory - Freiburg, Germany  
Center for Human Genetics, Inc - Cambridge, MA, USA  
Children's University Hospital, Human Genetics - Berne, Switzerland• Mutation scanning of the entire coding region
  
City of Hope National Medical Center, Clinical Molecular Diagnostic Laboratory - Duarte, CA, USA  
Connective Tissue Gene Tests - Allentown, PA, USA  
Correlagen Diagnostics, Inc. - Westborough, MA, USA  
GeneDx - Gaithersburg, MD, USA  
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA  
Health Care Center GENOMED, Laboratory of Human Genetics - Warsaw, Poland  
Health in Code S.L. - A Coruña, Spain  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Mayo Clinic - Minnesota, Cardiovascular Laboratory Medicine Genetics - Rochester, MN, USA  
MEDGEN, Genetic Diagnostics Laboratory - Warsaw, Poland  
St George's University of London, SW Thames Molecular Genetics Diagnostic Laboratory - London, Great Britain  
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany  
University of Washington Medical Center, Collagen Diagnostic Laboratory - Seattle, WA, 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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