Ahmad W - Search Results

1

Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindred.

Ahmad M, Faiyaz Ul Haque M, Ahmad W, Abbas H, Haque S, Krakow D, Rimoin DL, Lachman RS, Cohn DH. Ahmad M, et al. Among authors: ahmad w. Am J Med Genet. 1998 Aug 6;78(5):468-73. Am J Med Genet. 1998. PMID: 9714015

2

Alopecia universalis associated with a mutation in the human hairless gene.

Ahmad W, Faiyaz ul Haque M, Brancolini V, Tsou HC, ul Haque S, Lam H, Aita VM, Owen J, deBlaquiere M, Frank J, Cserhalmi-Friedman PB, Leask A, McGrath JA, Peacocke M, Ahmad M, Ott J, Christiano AM. Ahmad W, et al. Among authors: ahmad m. Science. 1998 Jan 30;279(5351):720-4. doi: 10.1126/science.279.5351.720. Science. 1998. PMID: 9445480

3

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

Ahmad W, Brancolini V, ul Faiyaz MF, Lam H, ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM. Ahmad W, et al. Among authors: ahmad m. Am J Hum Genet. 1998 Apr;62(4):987-91. doi: 10.1086/301799. Am J Hum Genet. 1998. PMID: 9529357 Free PMC article. No abstract available.

4

A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad M, McGrath JA, Christiano AM. Ahmad W, et al. Among authors: ahmad m. Am J Hum Genet. 1998 Oct;63(4):984-91. doi: 10.1086/302069. Am J Hum Genet. 1998. PMID: 9758627 Free PMC article.

5

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse.

Faiyaz ul Haque M, King LM, Krakow D, Cantor RM, Rusiniak ME, Swank RT, Superti-Furga A, Haque S, Abbas H, Ahmad W, Ahmad M, Cohn DH. Faiyaz ul Haque M, et al. Among authors: ahmad w, ahmad m. Nat Genet. 1998 Oct;20(2):157-62. doi: 10.1038/2458. Nat Genet. 1998. PMID: 9771708

6

Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.

Ahmad W, Zlotogorski A, Panteleyev AA, Lam H, Ahmad M, Faiyaz ul Haque M, Abdallah HM, Dragan L, Christiano AM. Ahmad W, et al. Among authors: ahmad m. Genomics. 1999 Mar 1;56(2):141-8. doi: 10.1006/geno.1998.5699. Genomics. 1999. PMID: 10051399 Free article.

7

Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.

Ahmad W, De Fusco M, Faiyaz ul Haque M, Aridon P, Sarno T, Sohail M, ul Haque S, Ahmad M, Ballabio A, Franco B, Casari G. Ahmad W, et al. Among authors: ahmad m. Eur J Hum Genet. 1999 Oct-Nov;7(7):828-32. doi: 10.1038/sj.ejhg.5200376. Eur J Hum Genet. 1999. PMID: 10573017

8

Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.

Ahmad W, Noci S, Faiyaz ul Haque M, Sarno T, Aridon P, Ahmad MM, Amin-Ud-Din M, Rafiq MA, ul Haque S, De Fusco M, Ballabio A, Franco B, Casari G. Ahmad W, et al. Among authors: ahmad mm. Am J Med Genet. 2001 Apr 15;100(1):62-5. doi: 10.1002/1096-8628(20010415)100:1<62::aid-ajmg1190>3.0.co;2-h. Am J Med Genet. 2001. PMID: 11337751

9

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. Among authors: ahmad w, ahmad m. Clin Genet. 2002 Jun;61(6):454-8. doi: 10.1034/j.1399-0004.2002.610610.x. Clin Genet. 2002. PMID: 12121354

10

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. Among authors: ahmad w, ahmad m. Am J Med Genet. 2002 Jul 22;111(1):31-7. doi: 10.1002/ajmg.10501. Am J Med Genet. 2002. PMID: 12124730 Review.

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