Pham T - Search Results

1

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: pham t. 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.

2

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. Hum Hered. 2003;55(1):71-4. doi: 10.1159/000071813. Hum Hered. 2003. PMID: 12890929 Free PMC article.

3

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. 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.

4

DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.

Ansar M, Chahrour MH, Amin Ud Din M, Arshad M, Haque S, Pham TL, Yan K, Ahmad W, Leal SM. Ansar M, et al. Hum Hered. 2004;57(4):195-9. doi: 10.1159/000081446. Hum Hered. 2004. PMID: 15583425 Free PMC article.

5

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.

Mir A, Ansar M, Chahrour MH, Pham TL, Wajid M, Haque S, Yan K, Ahmad W, Leal SM. Mir A, et al. Am J Med Genet A. 2005 Feb 15;133A(1):23-6. doi: 10.1002/ajmg.a.30516. Am J Med Genet A. 2005. PMID: 15637723 Free PMC article.

6

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.

Aslam M, Wajid M, Chahrour MH, Ansar M, Haque S, Pham TL, Santos RP, Yan K, Ahmad W, Leal SM. Aslam M, et al. Am J Med Genet A. 2005 Feb 15;133A(1):18-22. doi: 10.1002/ajmg.a.30508. Am J Med Genet A. 2005. PMID: 15641023 Free PMC article.

7

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. 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.

8

Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.

Santos RL, Wajid M, Pham TL, Hussan J, Ali G, Ahmad W, Leal SM. Santos RL, et al. Among authors: pham tl. Clin Genet. 2005 Jan;67(1):61-8. doi: 10.1111/j.1399-0004.2005.00379.x. Clin Genet. 2005. PMID: 15617550 Free PMC article.

9

Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.

Santos RL, El-Shanti H, Sikandar S, Lee K, Bhatti A, Yan K, Chahrour MH, McArthur N, Pham TL, Mahasneh AA, Ahmad W, Leal SM. Santos RL, et al. J Mol Med (Berl). 2006 Mar;84(3):226-31. doi: 10.1007/s00109-005-0015-3. Epub 2005 Dec 31. J Mol Med (Berl). 2006. PMID: 16389551 Free PMC article.

10

Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.

Santos RL, Wajid M, Khan MN, McArthur N, Pham TL, Bhatti A, Lee K, Irshad S, Mir A, Yan K, Chahrour MH, Ansar M, Ahmad W, Leal SM. Santos RL, et al. Hum Mutat. 2005 Oct;26(4):396. doi: 10.1002/humu.9374. Hum Mutat. 2005. PMID: 16134132 Free PMC article.

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