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Browsing by Author Chaudhry, A

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	Title	Author(s)	Issue Date
	Agenesis of the corpus callosum, Developmental delay, Autism spectrum disorder, facial dysmorphism, and Posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion Journal:American Journal of Medical Genetics Part A	Chaudhry, A Chung, BHY Stavropoulos, DJ Araya, MP Ali, A Heon, E Chitayat, D	2017
	Phenotypic spectrum associated with PTCHD1 deletion and truncating mutations includes intellectual disability and autism spectrum disorder Journal:Clinical Genetics	Chaudhry, A Noor, A Degagne, B Baker, K Bok, LA Brady, AF Chitayat, D Chung, BHY Cytrynbaum, C Dyment, D Filges, I Helm, B Hutchison, HT Jeng, LJB Laumonnier, F Marshall, CR Menzel, M Parkash, S Parker, MJ The, DDD STUDY Raymond, FL Rideout, AL Roberts, W Rupps, R Schanze, I Schrander-Stumpel, CTRM Speevak, MD Stavropoulos, DJ Stevens, SJC Thomas, ERA Toutain, A Vergano, S Weksberg, R Scherer, SW Vincent, JB Carter, MT	2015

Showing results 1 to 2 of 2