Disorders


 

SOST-Related Sclerosing Bone Dysplasias


 

GeneReviewOMIM

GeneLocusProtein
SOST17q12-q21Sclerostin

Laboratory Test Method Prenatal Carrier *
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, 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
• Targeted mutation analysis

* 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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