Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly-Reference-Cited by-同舟云学术

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Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly

Published:2016-05-25 Issue:5 Volume:11 Page:e0155180
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Deng Hao,Deng Sheng,Xu Hongbo,Deng Han-Xiang,Chen Yulan,Yuan Lamei,Deng Xiong,Yang Shengbo,Guan Liping,Zhang Jianguo,Yuan Hong,Guo Yi

Funder

Construction Fund for Key Subjects of the Third Xiangya Hospital, Central South University, China

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province, China

Postgraduates Innovative Pilot Scheme of Hunan Province, China

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

1. Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred;S Malik;Eur J Hum Genet,2008

2. Congenital anomalies of the hand: an overview;JM Linder;J Craniofac Surg,2009

3. Reconstruction of congenital differences of the hand;SJ Bates;Plast Reconstr Surg,2009

4. Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome;LE Figuera;Clin Dysmorphol,2002

5. A girl with 15q overgrowth syndrome and dup(15)(q24q26.3) that included telomeric sequences;L Gutierrez-Franco Mde;Korean J Lab Med,2010

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