Disorders


 

10p13-p14 Deletion Syndrome


 

OMIM


Laboratory Test Method Prenatal Carrier *
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA• FISH-metaphase
  
Boston Children's Hospital, Genetics Diagnostic Laboratory - Waltham, MA, USA• Deletion/duplication analysis
  
Brigham and Women's Hospital, Center for Advanced Molecular Diagnostics, Cytogenetics Laboratory - Boston, MA, USA• FISH-metaphase
  
CGC Genetics - Porto, Portugal• Deletion/duplication analysis
 
Cincinnati Children's Hospital Medical Center, Cytogenetics Laboratory - Cincinnati, OH, USA• FISH-metaphase
 
CytoGenX - Stony Brook, NY, USA• FISH-metaphase
 
PerkinElmer, Signature Genomic Laboratories - Spokane, WA, USA• FISH-metaphase
 
University of Colorado Anschutz Medical Campus, Colorado Genetics Laboratory - Denver, CO, USA• FISH-metaphase
 
University of Oklahoma Health Sciences Center, Genetics Laboratory - Oklahoma City, OK, USA• FISH-metaphase
 

* 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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