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Showing results 1 to 12 of 12

	Title	Author(s)	Issue Date	Views
	A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 Journal:Clinical Genetics	Zaidi, SHE Peltekova, V Meyer, S Lindinger, A Paterson, AD Tsui, LC FaiyazUlHaque, M Teebi, AS	2005	164
	Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes Journal:Clinical Genetics	FaiyazUlHaque, M Zaidi, SHE King, LM Haque, S Patel, M Ahmad, M Siddique, T Ahmad, W Tsui, LC Cohn, DH	2005	131
	Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia Journal:American Journal of Medical Genetics	FaiyazUlHaque, M Ahmad, W Wahab, A Haque, S Azim, AC Zaidi, SHE Teebi, AS Ahmad, M Cohn, DH Siddique, T Tsui, LC	2002	192
	Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families Journal:Clinical Genetics	FaiyazulHaque, M Zaidi, SHE Wahab, AA Eltohami, A AlMureikhi, MS AlThani, G Peltekova, VD Tsui, LC Teebi, AS	2008	177
	The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23 Journal:Clinical Genetics	Lo, B FaiyazUlHaque, M Banwell, B Blaser, S Paterson, AD Tsui, LC Teebi, AS	2004	146
	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	178
	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	155
	A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1 Journal:Journal of Investigative Dermatology	Rafiq, MA FaiyazulHaque, M Ud Din, MA Malik, S Sohail, M Anwar, M Haque, S Paterson, AD Tsui, LC Ahmad, W	2005	128
	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	168
	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	182
	Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism Journal:American Journal of Medical Genetics	Lo, B FaiyazUlHaque, M Kennedy, S Aviv, R Tsui, LC Teebi, AS	2003	175
	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	175

Showing results 1 to 12 of 12