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Items: 6

1.
Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
Limeng Dai, Dan Liu, Min Song, Xueqing Xu, Gang Xiong, Kang Yang, Kun Zhang, Hui Meng, Hong Guo, Yun Bai
PLoS One. 2014; 9(5): e96192. Published online 2014 May 1. doi: 10.1371/journal.pone.0096192
Correction in:
PLoS One. 2014; 9(7): e104309.
PMCID:
PMC4006867
ArticlePDF–828K
2.
Gap junctions in inherited human disorders of the central nervous system
Charles K. Abrams, Steven S. Scherer
Biochim Biophys Acta. Author manuscript; available in PMC 2013 Sep 12.
Published in final edited form as: Biochim Biophys Acta. 2012 Aug; 1818(8): 2030–2047. Published online 2011 Aug 16. doi: 10.1016/j.bbamem.2011.08.015
PMCID:
PMC3771870
ArticlePDF–1.5M
3.
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.
F Goodman, M L Giovannucci-Uzielli, C Hall, W Reardon, R Winter, P Scambler
Am J Hum Genet. 1998 Oct; 63(4): 992–1000. doi: 10.1086/302070
PMCID:
PMC1377502
SummaryPDF–828K
4.
Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36
Kristin Bosse, Regina C. Betz, Young-Ae Lee, Thomas F. Wienker, André Reis, Heidi Kleen, Peter Propping, Sven Cichon, Markus M. Nöthen
Am J Hum Genet. 2000 Aug; 67(2): 492–497. Published online 2000 Jun 30. doi: 10.1086/303028
PMCID:
PMC1287194
ArticlePDF–591K
5.
Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?
E F Percin, S Percin, H Egilmez, I Sezgin, F Ozbas, A N Akarsu
J Med Genet. 1998 Oct; 35(10): 868–874. doi: 10.1136/jmg.35.10.868
PMCID:
PMC1051468
ArticlePDF–1.6M
6.
Problem of sex ratio in cases of type I syndactyly.
C M Woolf, D L Cone
J Med Genet. 1977 Apr; 14(2): 108–113. doi: 10.1136/jmg.14.2.108
PMCID:
PMC1013524
ArticlePDF–798K

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