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Consanguinity: A blessing or menace at population level?
Bhinder MA, Sadia H, Mahmood N, Qasim M, Hussain Z, Rashid MM, Zahoor MY, Bhatti R, Shehzad W, Waryah AM, Jahan S. Bhinder MA, et al. Ann Hum Genet. 2019 Jul;83(4):214-219. doi: 10.1111/ahg.12308. Epub 2019 Mar 19. Ann Hum Genet. 2019. PMID: 30891741 Review.
Molecular and clinical studies of X-linked deafness among Pakistani families.
Waryah AM, Ahmed ZM, Bhinder MA, Choo DI, Sisk RA, Shahzad M, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Waryah AM, et al. Among authors: bhinder ma. J Hum Genet. 2011 Jul;56(7):534-40. doi: 10.1038/jhg.2011.55. Epub 2011 Jun 2. J Hum Genet. 2011. PMID: 21633365 Free PMC article.
Junctional Epidermolysis Bullosa (Non-Herlitz Type).
Bhinder MA, Arshad MW, Zahoor MY, Shehzad W, Tariq M, Shabbir MI. Bhinder MA, et al. J Coll Physicians Surg Pak. 2017 May;27(5):308-310. J Coll Physicians Surg Pak. 2017. PMID: 28599695
Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients.
Waryah YM, Iqbal M, Sheikh SA, Baig MA, Narsani AK, Atif M, Bhinder MA, Ur Rahman A, Memon AI, Pirzado MS, Waryah AM. Waryah YM, et al. Among authors: bhinder ma. Int J Ophthalmol. 2019 Jan 18;12(1):8-15. doi: 10.18240/ijo.2019.01.02. eCollection 2019. Int J Ophthalmol. 2019. PMID: 30662834 Free PMC article.
23 results