Mehdi SQ - Search Results

1

Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.

Abid A, Akhtar N, Khaliq S, Mehdi SQ. Abid A, et al. Among authors: mehdi sq. J Coll Physicians Surg Pak. 2011 Apr;21(4):202-6. J Coll Physicians Surg Pak. 2011. PMID: 21453614

2

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

Forshew T, Johnson CA, Khaliq S, Pasha S, Willis C, Abbasi R, Tee L, Smith U, Trembath RC, Mehdi SQ, Moore AT, Maher ER. Forshew T, et al. Among authors: mehdi sq. Hum Genet. 2005 Sep;117(5):452-9. doi: 10.1007/s00439-005-1309-9. Epub 2005 Jun 16. Hum Genet. 2005. PMID: 15959809

3

Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children.

Shahid S, Abid A, Mehdi SQ, Firasat S, Lanewala A, Naqvi SA, Rizvi SA, Khaliq S. Shahid S, et al. Among authors: mehdi sq. Gene. 2012 Feb 1;493(1):165-8. doi: 10.1016/j.gene.2011.10.016. Epub 2011 Oct 15. Gene. 2012. PMID: 22033511

4

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.

Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ. Abid A, et al. Among authors: mehdi sq. Gene. 2012 Jul 10;502(2):133-7. doi: 10.1016/j.gene.2012.04.063. Epub 2012 Apr 28. Gene. 2012. PMID: 22565185

5

The effect of chemokine receptor gene polymorphisms (CCR2V64I, CCR5-59029G>A and CCR5Δ32) on renal allograft survival in Pakistani transplant patients.

Firasat S, Raza A, Abid A, Aziz T, Mubarak M, Naqvi SA, Rizvi SA, Mehdi SQ, Khaliq S. Firasat S, et al. Among authors: mehdi sq. Gene. 2012 Dec 15;511(2):314-9. doi: 10.1016/j.gene.2012.09.099. Epub 2012 Oct 4. Gene. 2012. PMID: 23041556

6

HLA class I and II polymorphisms in the Gujjar population from Pakistan.

Raza A, Firasat S, Khaliq S, Abid A, Shah SS, Mehdi SQ, Mohyuddin A. Raza A, et al. Among authors: mehdi sq. Immunol Invest. 2013;42(8):691-700. doi: 10.3109/08820139.2013.806541. Epub 2013 Jul 11. Immunol Invest. 2013. PMID: 23845092 Review.

7

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

Khaliq S, Ajaz S, Firasat S, Shahid S, Hasan AS, Sultan G, Mohsin R, Hashmi A, Mubarak M, Naqvi SA, Rizvi SA, Mehdi SQ, Abid A. Khaliq S, et al. Among authors: mehdi sq. Mutat Res. 2014 May-Jun;763-764:45-52. doi: 10.1016/j.mrfmmm.2014.03.008. Epub 2014 Apr 12. Mutat Res. 2014. PMID: 24727139 Clinical Trial.

8

The Kalash genetic isolate: ancient divergence, drift, and selection.

Ayub Q, Mezzavilla M, Pagani L, Haber M, Mohyuddin A, Khaliq S, Mehdi SQ, Tyler-Smith C. Ayub Q, et al. Among authors: mehdi sq. Am J Hum Genet. 2015 May 7;96(5):775-83. doi: 10.1016/j.ajhg.2015.03.012. Epub 2015 Apr 30. Am J Hum Genet. 2015. PMID: 25937445 Free PMC article.

9

Mutation screening of Pakistani families with congenital eye disorders.

Khaliq S, Abid A, Hameed A, Anwar K, Mohyuddin A, Azmat Z, Shami SA, Ismail M, Mehdi SQ. Khaliq S, et al. Among authors: mehdi sq. Exp Eye Res. 2003 Mar;76(3):343-8. doi: 10.1016/s0014-4835(02)00304-4. Exp Eye Res. 2003. PMID: 12573663

10

Locus heterogeneity and Knobloch syndrome.

Joyce S, Tee L, Abid A, Khaliq S, Mehdi SQ, Maher ER. Joyce S, et al. Among authors: mehdi sq. Am J Med Genet A. 2010 Nov;152A(11):2880-1. doi: 10.1002/ajmg.a.33619. Am J Med Genet A. 2010. PMID: 20979194 No abstract available.

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

113 results

Search Page

Filters