Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation-Reference-Cited by-同舟云学术

Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation

Published:2017-06 Issue:6 Volume:21 Page:357-362
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Cao Lihua¹,Yang Wei²,Wang Shusen¹,Chen Chen¹,Zhang Xue¹²,Luo Yang¹

Affiliation:

1. The Research Center for Medical Genomics, Key Laboratory of Cell Biology, Ministry of Public Health, Key Laboratory of Medical Cell Biology, Ministry of Education, China Medical University, Shenyang, China.

2. McKusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2016.0415

Reference24 articles.

1. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly

2. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance

3. Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

4. Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation

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