Disorders


 

Bare Lymphocyte Syndrome, Type II, Complementation Group D


 

OMIM

GeneLocusProtein
RFXAP13q14Regulatory factor X-associated protein

Laboratory Test Method Prenatal Carrier *
GENETAQ, Molecular Genetics Centre - Malaga, Spain• 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.

Loading...