A Recessive Form of Ectrodactyly, and its Implications in Genetic Counseling
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,Biotechnology
Link
http://academic.oup.com/jhered/article-pdf/62/1/53/2668060/62-1-53.pdf
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Bilateral split hand foot malformation in siblings: Case series;International Journal of Surgery Case Reports;2018
2. HeterozygousDLX5nonsense mutation associated with isolated split-hand/foot malformation with reduced penetrance and variable expressivity in two unrelated families;Birth Defects Research Part A: Clinical and Molecular Teratology;2014-09-05
3. Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families;Orphanet Journal of Rare Diseases;2014-07-29
4. Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization;American Journal of Medical Genetics Part A;2011-04-11
5. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance;American Journal of Medical Genetics Part A;2010-07-15
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