1Sarkar S,Patra C,Dasgupta MK,et al.Prevalence of congenital anomalies in neonates and associated risk factors in a tertiary care hospital in eastern India[J].J Clin Neonatol,2013,2(3):131-134.
2Wang Z,Wang J,Li Y.Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial Polydactyly patients[J].Clin Chim Acta,2014,22(433):195-199.
4Boeing M,Paiva-Lde C,Garcias-Gde L,et al.Epidemiology of polydactylies:a case-control study in the population of Pelotas-RS[J].J Pediatr(Rio J),2001,77(2):148-152.
5Castilla EE,Lugarinho da Fonseca R,et al.Epidemiological analysis of rare polydactylies[J].Am J Med Genet,1996,65(4):295-303.
6Temtamy SA,Mc Kusick VA.The genetics of hand malformations[J].Birth Defects Orig Artic Ser,1978,14(3):1-619.
7Watson BT,Hennrikus WL.Postaxial type-B polydactyly-prevalence and treat-ment[J].J Bone Joint Surg Am,1997,79(1):65-68.
3Cetik O, Uslu M, Cirpar M, et al. Experience with the surgicaltreatment of radial polydactyly in adults. Annals Plastic Surgery, 2005,55 (4) : 363-366.
4Duchesne A, Gautier M, Chadi S, et al. Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle. Genomics, 2006,88 ( 5 ) : 610-621.
5Horsnell K, Ali M, Malik S, et al. Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion. Eur J Med Genet, 2006,49(5) : 396-401.
6Radhakrishna U, Blouin JL, Mehenni H, et al. Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis. Am J Hum Genet, 1997,60(3 ) : 597-604.
7Goode DK, Snell P, Smith SF, et al. Highly conserved regulatory elements around the SHH gene may contribute to the maintenance of conserved synteny across human chromosome 7q36.3. Genomics, 2005,86(2) : 172-181.
8Rogers JF. Clinical delineation of proximal and distal partial 13q trisomy. Clin Genet, 1984,25(3) :221-229.
9Sato D, Liang D, Wu L, et al. A syndactyly type IV locus maps to 7q36. J Hum Genet,2007,52(6) :561-564.
10Abbasi AA, Paparidis Z, Malik S, et al. Human GLI3 intragenic conserved non-coding sequences are tissue-specific enhancers. PLoS ONE,2007,2(4) :e366.