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Items: 3

1.

Association of vitamin D deficiency and VDBP gene polymorphism with the risk of AMI in a Pakistani population.

Mubashir M, Anwar S, Tareen AK, Mehboobali N, Iqbal K, Iqbal MP.

Pak J Med Sci. 2017 Nov-Dec;33(6):1349-1354. doi: 10.12669/pjms.336.13379.

2.

Genetic causes of moderate to severe hearing loss point to modifiers.

Naz S, Imtiaz A, Mujtaba G, Maqsood A, Bashir R, Bukhari I, Khan MR, Ramzan M, Fatima A, Rehman AU, Iqbal M, Chaudhry T, Lund M, Brewer CC, Morell RJ, Friedman TB.

Clin Genet. 2017 Apr;91(4):589-598. doi: 10.1111/cge.12856. Epub 2016 Oct 6.

3.

Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in Pakistan.

Salman M, Bashir R, Imtiaz A, Maqsood A, Mujtaba G, Iqbal M, Naz S.

Eur Arch Otorhinolaryngol. 2015 Aug;272(8):2071-5. doi: 10.1007/s00405-015-3523-y. Epub 2015 Jan 31.

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