(PDF) A Novel Homozygous Missense Mutation in BHLHA9 Causes

A Novel Homozygous Missense Mutation in BHLHA9 Causes Mesoaxial Synostotic Syndactyly With Phalangeal Reduction in a Pakistani Family

Human Genome Variation - United Kingdom

doi 10.1038/hgv.2017.54

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Molecular Biology

Date

December 1, 2017

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Publisher

Springer Science and Business Media LLC

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