Ahmad W - Search Results

1

Disease causing homozygous variants in the human hairless gene.

Mehmood S, Jan A, Raza SI, Ahmad F, Younus M, Irfanullah, Shahi S, Ayub M, Khan S, Ahmad W. Mehmood S, et al. Among authors: ahmad w, ahmad f. Int J Dermatol. 2016 Sep;55(9):977-81. doi: 10.1111/ijd.13109. Epub 2015 Dec 18. Int J Dermatol. 2016. PMID: 26680117

2

A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions.

Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM. Aita VM, et al. Among authors: ahmad w. Exp Dermatol. 2000 Apr;9(2):157-62. doi: 10.1034/j.1600-0625.2000.009002157.x. Exp Dermatol. 2000. PMID: 10772391

3

Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.

Ansar M, Ramzan M, Pham TL, Yan K, Jamal SM, Haque S, Ahmad W, Leal SM. Ansar M, et al. Among authors: ahmad w. Hum Hered. 2003;55(1):71-4. doi: 10.1159/000071813. Hum Hered. 2003. PMID: 12890929 Free PMC article.

4

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.

Wajid M, Abbasi AA, Ansar M, Pham TL, Yan K, Haque S, Ahmad W, Leal SM. Wajid M, et al. Among authors: ahmad w. Eur J Hum Genet. 2003 Oct;11(10):812-5. doi: 10.1038/sj.ejhg.5201041. Eur J Hum Genet. 2003. PMID: 14512973 Free PMC article.

5

A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1.

Rafiq MA, Faiyaz-Ul-Haque M, Ud Din MA, Malik S, Sohail M, Anwar M, Haque S, Paterson AD, Tsui LC, Ahmad W. Rafiq MA, et al. Among authors: ahmad w. J Invest Dermatol. 2005 Feb;124(2):338-42. doi: 10.1111/j.0022-202X.2004.23594.x. J Invest Dermatol. 2005. PMID: 15675952 Free article.

6

Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.

Naeem M, Muhammad D, Ahmad W. Naeem M, et al. Among authors: ahmad w. Br J Dermatol. 2005 Jul;153(1):46-50. doi: 10.1111/j.1365-2133.2005.06642.x. Br J Dermatol. 2005. PMID: 16029325

7

Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene.

John P, Aslam M, Rafiq MA, Amin-ud-din M, Haque S, Ahmad W. John P, et al. Among authors: ahmad w. Arch Dermatol Res. 2005 Nov;297(5):226-30. doi: 10.1007/s00403-005-0593-5. Epub 2005 Nov 11. Arch Dermatol Res. 2005. PMID: 16211417

8

Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3.

John P, Ali G, Chishti MS, Naqvi SM, Leal SM, Ahmad W. John P, et al. Among authors: ahmad w. Hum Genet. 2006 Jan;118(5):665-7. doi: 10.1007/s00439-005-0086-9. Epub 2005 Nov 5. Hum Genet. 2006. PMID: 16273389 Free PMC article.

9

A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly.

Gul A, Hassan MJ, Hussain S, Raza SI, Chishti MS, Ahmad W. Gul A, et al. Among authors: ahmad w. J Hum Genet. 2006;51(9):760-764. doi: 10.1007/s10038-006-0017-1. Epub 2006 Aug 10. J Hum Genet. 2006. PMID: 16900296

10

Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.

Wali A, Ansar M, Khan MN, Ahmad W. Wali A, et al. Among authors: ahmad w. Clin Exp Dermatol. 2006 Sep;31(5):695-8. doi: 10.1111/j.1365-2230.2006.02165.x. Clin Exp Dermatol. 2006. PMID: 16901311

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