Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation

Author:

Dai Li,Deng Ying,Li Nana,Xie Liang,Mao Meng,Zhu Jun

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Duijf PH, van Bokhoven H, Brunner HG: Pathogenesis of split-hand/split-foot malformation. Hum Mol Genet. 2003, 12: R51-R60. 10.1093/hmg/ddg090. Spec No 1

2. Elliott AM, Reed MH, Chudley AE, Chodirker BN, Evans JA: Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba. Canada Am J Med Genet A. 2006, 140 (13): 1428-1439.

3. Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S, Stephens K, Pagon RA, Patton MA: Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1. Am J Hum Genet. 1994, 55 (1): 12-20.

4. Faiyaz-Ul-Haque M, Zaidi SH, King LM, Haque S, Patel M, Ahmad M, Siddique T, Ahmad W, Tsui LC, Cohn DH: Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes. Clin Genet. 2005, 67 (1): 93-97.

5. Faiyaz U, Haque M, Uhlhaas S, Knapp M, Schuler H, Friedl W, Ahmad M, Propping P: Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1. Hum Genet. 1993, 91: 17-19.

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