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VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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Description

Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome

Mutations in this gene cause cranioectodermal dysplasia-1

Diseases associated with CEBPB includeShort-Rib Thoracic Dysplasia 1 With Or Without PolydactylyandShort-Rib Thoracic Dysplasia 2 With Or Without Polydactyly

This zinc finger gene has been identified at the breakpoints of a recurrent chromosomal translocation reported in endometrial stromal sarcoma

VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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