Clinical, genetic, and molecular aspects of split-hand/foot malformation: An update
Author:
Affiliation:
1. Istituto di Genetica Medica; Università Cattolica del Sacro Cuore; Rome Italy
2. Greenwood Genetic Center; Greenwood; South Carolina
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36239/fullpdf
Reference117 articles.
1. X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred;Ahmad;Hum Genet,1987
2. 17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD);Armour;Eur J Hum Genet,2011
3. Split hand-foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion-evidence for further heterogeneity;Aten;Am J Med Genet Part A,2009
4. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation;Babbs;Hum Genet,2007
5. The expanding panorama of split hand foot malformation;Basel;Am J Med Genet Part A,2006
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