Disorders


 

Paget Disease of Bone


 

OMIM

GeneLocusProtein
TNFRSF11A18q22.1Tumor necrosis factor receptor superfamily member 11A

Laboratory Test Method Prenatal Carrier *
Innovagenomics S.L, Innovagenomics - Salamanca, Spain• 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
 
University of Antwerp, Department of Medical Genetics - Van Hul Lab - Antwerp, Belgium• Sequence analysis of the entire coding region
• Linkage analysis
• Mutation scanning of select exons
 
University of California, Irvine, MitoMed Diagnostic Laboratory - Irvine, CA, USA• 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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