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Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma.
Micheal S, Ayub H, Islam F, Siddiqui SN, Khan WA, Akhtar F, Qamar R, Khan MI, den Hollander AI. Micheal S, et al. Among authors: ayub h. PLoS One. 2015 Dec 29;10(12):e0145005. doi: 10.1371/journal.pone.0145005. eCollection 2015. PLoS One. 2015. PMID: 26713451 Free PMC article.
The genetic spectrum of familial hypercholesterolemia in Pakistan.
Ahmed W, Whittall R, Riaz M, Ajmal M, Sadeque A, Ayub H, Qamar R, Humphries SE. Ahmed W, et al. Among authors: ayub h. Clin Chim Acta. 2013 Jun 5;421:219-25. doi: 10.1016/j.cca.2013.03.017. Epub 2013 Mar 25. Clin Chim Acta. 2013. PMID: 23535506 Free PMC article.
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
Shafique S, Siddiqi S, Schraders M, Oostrik J, Ayub H, Bilal A, Ajmal M, Seco CZ, Strom TM, Mansoor A, Mazhar K, Shah ST, Hussain A, Azam M, Kremer H, Qamar R. Shafique S, et al. Among authors: ayub h. PLoS One. 2014 Jun 20;9(6):e100146. doi: 10.1371/journal.pone.0100146. eCollection 2014. PLoS One. 2014. PMID: 24949729 Free PMC article.
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.
Maria M, Ajmal M, Azam M, Waheed NK, Siddiqui SN, Mustafa B, Ayub H, Ali L, Ahmad S, Micheal S, Hussain A, Shah ST, Ali SH, Ahmed W, Khan YM, den Hollander AI, Haer-Wigman L, Collin RW, Khan MI, Qamar R, Cremers FP. Maria M, et al. Among authors: ayub h. PLoS One. 2015 Mar 16;10(3):e0119806. doi: 10.1371/journal.pone.0119806. eCollection 2015. PLoS One. 2015. PMID: 25775262 Free PMC article.
53 results