Disorders


 

Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia


Synonym(s): Aspirin-Like Platelet Disorder, Familial Platelet Disorder with Associated Myeloid Malignancy

 

OMIM

GeneLocusProtein
RUNX121q22.3Runt-related transcription factor 1

Laboratory Test Method Prenatal Carrier *
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA• Sequence analysis of the entire coding region
  
BloodCenter of Wisconsin, Molecular Diagnostics Laboratory - Milwaukee, WI, USA• Sequence analysis of the entire coding region
 
Institute of Medical and Veterinary Science, Molecular Pathology - Adelaide, Australia• Sequence analysis of the entire coding region
 
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis
 
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands• Sequence analysis of the entire coding region
 
University Medical Center Utrecht, Genome Diagnostics Laboratory - Utrecht, Netherlands• Sequence analysis of the entire coding region
 

* 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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