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Browsing by Author Cohn, DH

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Showing results 1 to 5 of 5

	Title	Author(s)	Issue Date	Views
	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	166
	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	197
	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	190
	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	206
	Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations Journal:Journal of Medical Genetics	Aldinger, KA Mendelsohn, NJ Chung, BHY Zhang, W Cohn, DH Fernandez, B Alkuraya, FS Dobyns, WB Curry, CJ	2016	66

Showing results 1 to 5 of 5