Disorders

DFNX2 Nonsyndromic Hearing Loss and Deafness

Gene	Locus	Protein
POU3F4	Xq21.1

Laboratory	Test Method	Prenatal	Carrier *
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany
CGC Genetics - Porto, Portugal
GENETAQ, Molecular Genetics Centre - Malaga, Spain
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA
Hospital for Sick Children, Molecular Genetics Laboratory - Toronto, Canada
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands

^* 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.