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Browsing by Author Fernandez, B

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	Title	Author(s)	Issue Date
	Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion Journal:American Journal of Medical Genetics, Part A	Aldinger, KA Kogan, J Kimonis, V Fernandez, B Horn, D Klopocki, E Chung, B Toutain, A Weksberg, R Millen, KJ Barkovich, AJ Dobyns, WB	2013
	Correspondence: further studies on a kindred reported by Li 2009 as ‘A new syndrome of ankyloglossia and ulnar ray defects in Newfoundland kindred’. From ‘new syndrome’ through EEC to ulnar mammary syndrome (Letter to the Editor) Journal:Clinical Dysmorphology	Chung, BHY Fernandez, B Li, C Chitayat, D	2012
	Ulnar-Mammary Syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Jessen, J Chung, BHY Fernandez, B Li, C Chitayat, D	2010
	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

Showing results 1 to 4 of 4