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	Title	Author(s)	Issue Date	Views
	Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome) Journal:Clinical Genetics	FaiyazUlHaque, M Ahmad, W Zaidi, SHE Haque, S Teebi, AS Ahmad, M Cohn, DH Tsui, LC	2002	191
	Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar [5] Journal:Clinical Genetics	FaiyazUlHaque, M Zaidi, SHE AlMureikhi, MS Peltekova, I Tsui, LC Teebi, AS	2007
	A novel homozygous recessive mutation in the galactosyltransferase-I (B4GALT7) gene in individuals resembling the progeroid type of Ehlers-Danlos syndrome	Ul haque, MF Teebi, AS Al-ali, M Al-mureikhi, MS Kennedy, S Al-thani, G Zaidi, SHE Tsui, L-C	2003	117
	A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome Journal:Atherosclerosis	FaiyazUlHaque, M Zaidi, SHE AlSanna, N Alswaid, A Momenah, T Kaya, N AlDayel, F Bouhoaigah, I Saliem, M Tsui, LC Teebi, AS	2009
	A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type Journal:American Journal of Medical Genetics	FaiyazUlHaque, M Zaidi, SHE AlAli, M AlMureikhi, MS Kennedy, S AlThani, G Tsui, LC Teebi, AS	2004	111
	Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis) Journal:Clinical Genetics	FaiyazUlHaque, M Ahmad, W Zaidi, SHE Hussain, S Haque, S Ahmad, M Cohn, DH Tsui, LC	2004	194

Showing results 5 to 10 of 10 < previous