Disorders


 

Hereditary Congenital Facial Paresis 3


 

OMIM

GeneLocusProtein
HOXB117q21.32Homeobox protein Hox-B1

Laboratory Test Method Prenatal Carrier *
University Clinic Freiburg, Institute for Human Genetics - Freiburg, Germany• Sequence analysis of the entire coding region
• Deletion/duplication 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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