Ali G - Search Results

1

Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.

Khan S, Habib R, Mir H, Umm-e-Kalsoom, Naz G, Ayub M, Shafique S, Yamin T, Ali N, Basit S, Wasif N, Kamran-Ul-Hassan Naqvi S, Ali G, Wali A, Ansar M, Ahmad W. Khan S, et al. Among authors: ali n, ali g. Clin Exp Dermatol. 2011 Aug;36(6):652-4. doi: 10.1111/j.1365-2230.2011.04014.x. Epub 2011 Mar 21. Clin Exp Dermatol. 2011. PMID: 21426374

2

Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephaly.

Kousar R, Nawaz H, Khurshid M, Ali G, Khan SU, Mir H, Ayub M, Wali A, Ali N, Jelani M, Basit S, Ahmad W, Ansar M. Kousar R, et al. Among authors: ali n, ali g. J Child Neurol. 2010 Jun;25(6):715-20. doi: 10.1177/0883073809346850. Epub 2009 Oct 6. J Child Neurol. 2010. PMID: 19808985

3

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: ali g. 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

4

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: ali g. Clin Genet. 2007 Jul;72(1):23-9. doi: 10.1111/j.1399-0004.2007.00818.x. Clin Genet. 2007. PMID: 17594396

5

A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).

Jelani M, Wasif N, Ali G, Chishti M, Ahmad W. Jelani M, et al. Among authors: ali g. Clin Genet. 2008 Aug;74(2):184-8. doi: 10.1111/j.1399-0004.2008.01011.x. Epub 2008 Apr 28. Clin Genet. 2008. PMID: 18445047

6

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.

Tariq M, Ayub M, Jelani M, Basit S, Naz G, Wasif N, Raza SI, Naveed AK, ullah Khan S, Azeem Z, Yasinzai M, Wali A, Ali G, Chishti MS, Ahmad W. Tariq M, et al. Among authors: ali g. Br J Dermatol. 2009 May;160(5):1006-10. doi: 10.1111/j.1365-2133.2009.09046.x. Epub 2009 Mar 9. Br J Dermatol. 2009. PMID: 19292720

7

A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.

Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W. Khan S, et al. Among authors: ali n, ali g. Clin Genet. 2012 Jul;82(1):48-55. doi: 10.1111/j.1399-0004.2011.01698.x. Epub 2011 May 27. Clin Genet. 2012. PMID: 21554266

8

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. 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.

9

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: ali g. 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.

10

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: ali g. 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.

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

853 results

Search Page

Filters