2Sayli BS, Akarsu AN, Sayli U, etal. A large Turkish kindred with syndactyly type II (synpolydactyly):1 field investigation, clinical and pedigree data[ J]. J Med Genet, 1995, 32:421-434.
3Muragaki Y, Mundlos S, Upton J, et al. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 [ J]. Science, 1996, 272:548-551.
4Goodman FR, Mundlos S, Muragaki Y, et al. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract[J]. Proc Nail Acad Sci U S A, 1997, 94:7458-7463.
5Mundlos S, Otto F, Mundlos C, et al. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia [ J ]. Cell, 1997, 89:773-779.
6Brown SA, Warburton D, Brown LY, et al. Holoprosencephaly due tomutations in ZIC2, a homologue of Drosophila odd-paired [J]. Nat Genet, 1998, 20:180-183.
7Crisponi L, Deiana M, Loi A, et al. The putative forkheadtranscription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome[J]. Nat Genet, 2001, 27:159-166.
8A.N. Albrecht, U. Komak, A. B ddrich, et al. Associated polyalanine tract expansions [J]. Hum. Mol. Genet, 2004, 13 (20) :2351-2359.
9Bruneau, K.R. Johnson, M. Yamamoto, et al. The mouse Hoxdl3 spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disnJpts the function but not the expression of other Hoxd genes[J]. Dev Biol, 2001, 237:345- 353.
10Ktherine Horsnell, Manir Ali, Saghira Malik, et al. Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion [ J ]. European Journal of Medical Genetics, 2006, 49:396-401.
1David B, Lumenta MD, Hugo B, et al. Long-term outcomes of web creep, scar quality, and function after simple syndacty|y surgical treatment[ J ]. J Hand Surg,2010,35(8) :1323 - 1329.
2Adrian E, Flatt. Webbed fingers [ J ]. Baylor University medical center proceedings,2005,18 ( 1 ) :26 - 27.
