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Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 5, 2025
Fragile X syndrome: genetic and clinical profile in the Hong Kong Chinese populationC W M Au, H M Luk, S Ho, et al.Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|August 10, 2004
Chronic benign neutropenia among Chinese childrenB H Y Chung, G C F Chan, T L Lee, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 21, 2003
Klebsiella infection in patients with thalassemiaB H Y Chung, S Y Ha, G C F Chan, et al.Clinical Genetics|December 13, 2017
Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA-related overgrowth spectrumM E Michel, D J Konczyk, K S Yeung, et al.Prenatal Diagnosis|May 6, 2024
The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta-analysisK Reilly, S Sonner, N McCay, et al.Nature Communications|December 23, 2015
NSD1 mutations generate a genome-wide DNA methylation signatureS Choufani, C Cytrynbaum, B H Y Chung, et al.Clinical Genetics|December 15, 2017
Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansionA T G Chiu, S L C Pei, C C Y Mak, et al.Clinical Genetics|October 27, 2015
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and managementM Avila, D A Dyment, J V Sagen, et al.Pageof 1