TW01051/TW/FIC NIH HHS/United States[Grants and Funding] - Search Results

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Year	Number of Results
2002	2
2005	1
2024	0

Page 1

Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia.

Faiyaz-Ul-Haque M, Ahmad W, Wahab A, Haque S, Azim AC, Zaidi SH, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui LC. Faiyaz-Ul-Haque M, et al. Am J Med Genet. 2002 Jul 22;111(1):31-7. doi: 10.1002/ajmg.10501. Am J Med Genet. 2002. PMID: 12124730 Review.

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.

Faiyaz-Ul-Haque M, Zaidi SH, King LM, Haque S, Patel M, Ahmad M, Siddique T, Ahmad W, Tsui LC, Cohn DH. Faiyaz-Ul-Haque M, et al. Clin Genet. 2005 Jan;67(1):93-7. doi: 10.1111/j.1399-0004.2004.00369.x. Clin Genet. 2005. PMID: 15617554

Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome).

Faiyaz-Ul-Haque M, Ahmad W, Zaidi SH, Haque S, Teebi AS, Ahmad M, Cohn DH, Tsui LC. Faiyaz-Ul-Haque M, et al. Clin Genet. 2002 Jun;61(6):454-8. doi: 10.1034/j.1399-0004.2002.610610.x. Clin Genet. 2002. PMID: 12121354

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