Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type-Reference-Cited by-同舟云学术

Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type

Published:2014-12 Issue:6 Volume:95 Page:649-659
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Malik Sajid,Percin Ferda E.,Bornholdt Dorothea,Albrecht Beate,Percesepe Antonio,Koch Manuela C.,Landi Antonio,Fritz Barbara,Khan Rizwan,Mumtaz Sara,Akarsu Nurten A.,Grzeschik Karl-Heinz

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference37 articles.

1. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin;Malik;Am. J. Med. Genet. A.,2004

2. Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3;Malik;Am. J. Med. Genet. A.,2005

3. Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?;Percin;J. Med. Genet.,1998

4. Syndactyly: phenotypes, genetics and current classification;Malik;Eur. J. Hum. Genet.,2012

5. A simple method for characterising syndactyly in clinical practice;Malik;Genet. Couns.,2005

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