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Showing results 1 to 2 of 2

	Title	Author(s)	Issue Date
	Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature Journal:American Journal of Medical Genetics, Part A	Liu, APY Tang, WF Lau, ETK Chan, YK Kan, SYA Wong, KY Tso, WYW Jalal, K Lee, SL Chau, CSK Chung, BHY	2013
	A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - Is cardiac assessment necessary for all patients with 17p13.3 microduplication? Journal:European Journal of Medical Genetics	Ho, ACC Liu, APY Lun, KS Tang, WF Chan, KYK Lau, EYT Tang, MHY Tan, TY Chung, BHY	2012

Showing results 1 to 2 of 2