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Browsing by Author Qamar, R.

Full Text	Issue Date	Title	Author(s)
	2011	CLRN1 mutations cause nonsyndromic retinitis pigmentosa	Khan, M.I.; Kersten, F.F.J.; Azam, M.; Collin, R.W.J.; Hussain, A., et al
	2011	Antimicrobial Resistant Escherichia coli Strains Isolated From Food Animals in Pakistan.	Idrees, M.; Shah, M.A.; Micheal, S.; Qamar, R.; Bokhari, H.
	2011	Identification of novel mutations in pakistani families with autosomal recessive retinitis pigmentosa	Azam, M.; Collin, R.W.J.; Malik, A.; Khan, M.I.; Shah, S.T., et al
	2011	XRCC1 and XPD DNA repair gene polymorphisms: a potential risk factor for glaucoma in the Pakistani population	Yousaf, S.; Khan, M.I.; Micheal, S.; Akhtar, F.; Ali, S.H., et al
	2010	Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa.	Bandah-Rozenfeld, D.; Collin, R.W.J.; Banin, E.; Born, L.I. van den; Coene, K.L.M., et al
	2010	The association of glutathione S-transferase GSTT1 and GSTM1 gene polymorphism with pseudoexfoliative glaucoma in a Pakistani population.	Khan, M.I.; Micheal, S.; Akhtar, F.; Ahmed, W.; Ijaz, B., et al
	2010	Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa.	Khan, M.I.; Collin, R.W.J.; Arimadyo, K.; Micheal, S.; Azam, M., et al
	2010	Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia.	Ajmal, M.; Ahmed, W.; Sadeque, A.; Ali, S.H.; Bokhari, S.H., et al
	2010	Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia	Azam, M.; Collin, R.W.J.; Shah, S.T.; Shah, A.A.; Khan, M.I., et al
	2010	Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts	Ayub, H.; Khan, M.I.; Micheal, S.; Akhtar, F.; Ajmal, M., et al
	2009	Association of tumor necrosis factor alpha gene polymorphism G-308A with pseudoexfoliative glaucoma in the Pakistani population	Khan, M.I.; Micheal, S.; Rana, N.; Akhtar, F.; Hollander, A.I. den, et al
	2009	A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa	Azam, M.; Khan, M.I.; Gal, A.; Hussain, A.; Shah, S.T., et al
	2009	A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.	Azam, M.; Collin, R.W.J.; Khan, M.I.; Shah, S.T.; Qureshi, N., et al
	2009	MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma	Micheal, S.; Qamar, R.; Akhtar, F.; Khan, M.I.; Khan, W.A., et al
	2009	Association of ABO blood groups with glaucoma in the Pakistani population.	Khan, M.I.; Micheal, S.; Akhtar, F.; Naveed, A.; Ahmed, A., et al