Disorders


 

Mitochondrial DNA Deletion Syndromes


Synonym(s): mtDNA Deletion Syndromes

 

GeneReviewOMIM


Laboratory Test Method Prenatal Carrier *
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA  
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA• Enzyme assay
  
Center for Human Genetics, Inc - Cambridge, MA, USA  
Centre Hospitalier Universitaire de Grenoble, Biochimie Genetique et Molculaire - Grenoble, France• Enzyme assay
  
Columbia University, Molecular Neurogenetics Laboratory - New York, NY, USA  
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel  
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA  
GeneDx - Gaithersburg, MD, USA  
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Targeted mutation analysis
  
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands  
Medgene, MedGene - Bratislava, Slovakia  
Medical Neurogenetics - Atlanta, GA, USA  
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany  
Ohio State University, Molecular Pathology Laboratory - Columbus, OH, USA  
Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center - Portland, OR, USA  
Praxis fuer Humangenetik Wien - Vienna, Austria  
Pro Genetic, Inc, University Children's Genetics Laboratory - Glendale, CA, USA  
Rush University Medical Center, Genetics Laboratory - Department of Pathology - Chicago, IL, USA  
Sir Ganga Ram Hospital, Center of Medical Genetics - New Delhi, India  
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany  
Transgenomic, Transgenomic - Omaha - Omaha, NE, USA  
University of Alberta, Molecular Diagnostic Laboratory - Edmonton, Canada  
University of California, Irvine, MitoMed Diagnostic Laboratory - Irvine, CA, USA  
University of Turku, Diagnostic DNA Laboratory - Turku, Finland  

* 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.

Loading...