John P - Search Results

1

Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.

John P, Tariq M, Arshad Rafiq M, Amin-Ud-Din M, Muhammad D, Waheed I, Ansar M, Ahmad W. John P, et al. Arch Dermatol Res. 2006 Aug;298(3):135-7. doi: 10.1007/s00403-006-0671-3. Epub 2006 Jun 13. Arch Dermatol Res. 2006. PMID: 16770573

2

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. 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

3

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. 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.

4

The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23.

Ali G, Santos RL, John P, Wambangco MA, Lee K, Ahmad W, Leal S. Ali G, et al. Among authors: john p. Clin Genet. 2006 May;69(5):429-33. doi: 10.1111/j.1399-0004.2006.00611.x. Clin Genet. 2006. PMID: 16650082 Free PMC article.

5

A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.

Wali A, John P, Gul A, Lee K, Chishti MS, Ali G, Hassan MJ, Leal SM, Ahmad W. Wali A, et al. Among authors: john p. Clin Genet. 2006 Sep;70(3):233-9. doi: 10.1111/j.1399-0004.2006.00661.x. Clin Genet. 2006. PMID: 16922726 Free PMC article.

6

Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.

Naeem M, Jelani M, Lee K, Ali G, Chishti MS, Wali A, Gul A, John P, Hassan MJ, Leal SM, Ahmad W. Naeem M, et al. Among authors: john p. Br J Dermatol. 2006 Dec;155(6):1184-90. doi: 10.1111/j.1365-2133.2006.07509.x. Br J Dermatol. 2006. PMID: 17107387 Free PMC article.

7

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis.

Ali G, Chishti MS, Raza SI, John P, Ahmad W. Ali G, et al. Among authors: john p. Hum Genet. 2007 May;121(3-4):319-25. doi: 10.1007/s00439-007-0344-0. Epub 2007 Feb 27. Hum Genet. 2007. PMID: 17333281

8

Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.

Wali A, Ali G, John P, Lee K, Chishti MS, Leal SM, Ahmad W. Wali A, et al. Among authors: john p. Ann Hum Genet. 2007 Sep;71(Pt 5):570-7. doi: 10.1111/j.1469-1809.2007.00362.x. Epub 2007 Apr 19. Ann Hum Genet. 2007. PMID: 17451405 Free PMC article.

9

Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.

Naeem M, John P, Ali G, Ahmad W. Naeem M, et al. Among authors: john p. Clin Exp Dermatol. 2007 Sep;32(5):502-5. doi: 10.1111/j.1365-2230.2007.02413.x. Epub 2007 May 8. Clin Exp Dermatol. 2007. PMID: 17489990

10

Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.

Wali A, Chishti M, Ayub M, Yasinzai M, Kafaitullah, Ali G, John P, Ahmad W. Wali A, et al. Among authors: john p. Clin Genet. 2007 Jul;72(1):23-9. doi: 10.1111/j.1399-0004.2007.00818.x. Clin Genet. 2007. PMID: 17594396

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