Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2006.00620.x/fullpdf
Reference27 articles.
1. A simple method for characterising syndactyly in clinical practice;Malik;Genet Couns,2005
2. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data;Sayli;J Med Genet,1995
3. Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker;Sarfarazi;Hum Mol Genet,1995
4. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13;Muragaki;Science,1996
5. Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families;Akarsu;Hum Mol Genet,1996
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