Ahmad W - Search Results

1

Homozygous sequence variants in the NPR2 gene underlying Acromesomelic dysplasia Maroteaux type (AMDM) in consanguineous families.

Irfanullah, Umair M, Khan S, Ahmad W. Irfanullah, et al. Among authors: ahmad w. Ann Hum Genet. 2015 Jul;79(4):238-44. doi: 10.1111/ahg.12116. Epub 2015 May 11. Ann Hum Genet. 2015. PMID: 25959430

2

A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.

Ansar M, Din MA, Arshad M, Sohail M, Faiyaz-Ul-Haque M, Haque S, Ahmad W, Leal SM. Ansar M, et al. Among authors: ahmad w. Eur J Hum Genet. 2003 Jan;11(1):77-80. doi: 10.1038/sj.ejhg.5200905. Eur J Hum Genet. 2003. PMID: 12529709 Free PMC article.

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

A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.

Rafique MA, Ansar M, Jamal SM, Malik S, Sohail M, Faiyaz-Ul-Haque M, Haque S, Leal SM, Ahmad W. Rafique MA, et al. Among authors: ahmad w. Eur J Hum Genet. 2003 Aug;11(8):623-8. doi: 10.1038/sj.ejhg.5201005. Eur J Hum Genet. 2003. PMID: 12891384 Free PMC article.

5

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.

6

Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.

Rafiq MA, Ansar M, Pham T, Amin-ud-Din M, Anwar M, Haque S, Chahrour MH, Yan K, Leal SM, Ahmad W. Rafiq MA, et al. Among authors: ahmad w. Clin Genet. 2004 Jul;66(1):73-8. doi: 10.1111/j.0009-9163.2004.00273.x. Clin Genet. 2004. PMID: 15200512 Free PMC article.

7

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

8

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.

Irshad S, Santos RL, Muhammad D, Lee K, McArthur N, Haque S, Ahmad W, Leal SM. Irshad S, et al. Among authors: ahmad w. Clin Genet. 2005 Sep;68(3):262-7. doi: 10.1111/j.1399-0004.2005.00492.x. Clin Genet. 2005. PMID: 16098016 Free PMC article.

9

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

10

A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.

Hassan MJ, Santos RL, Rafiq MA, Chahrour MH, Pham TL, Wajid M, Hijab N, Wambangco M, Lee K, Ansar M, Yan K, Ahmad W, Leal SM. Hassan MJ, et al. Among authors: ahmad w. Hum Genet. 2006 Jan;118(5):605-10. doi: 10.1007/s00439-005-0079-8. Epub 2005 Oct 29. Hum Genet. 2006. PMID: 16261342 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,415 results

Search Page

Filters