Prenatal phenotype of Kabuki syndrome: A case series and literature review von So, Po Lam, Luk, Ho Ming, Cheung, Ka Wang, Hui, Winnie, Chung, Man Yan, Mak, Annisa S. L., Lok, Wing Yi, Yu, Kris Pui Tak, Cheng, Shirley S. W., Hau, Edgar W. L., Ho, Stephanie, Lam, Stephen T. S., Lo, Ivan F. M.

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Clinical and molecular characterization study of Chinese Kabuki syndrome in Hong Kong von So, Po L., Luk, Ho M., Yu, Kris P. T., Cheng, Shirley S.W., Hau, Edgar W. L., Ho, Stephanie K. L., Lam, Stephen T. S., Lo, Ivan F. M.

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Genotype/phenotype correlation in 123 Chinese patients with Tuberous Sclerosis Complex von Ng, Samuel YL, Luk, Ho-Ming, Hau, Edgar WL, Cheng, Shirley SW, Yu, Kris PT, Ho, Stephanie, Mok, Myth TS, Lo, Ivan FM

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Old and new perspectives on Neurofibromatosis type 1: Clinical and molecular characterization of 832 patients from a single centre over 16 years von Ho, Stephanie KL, Luk, Ho-ming, Ng, Samuel YL, Yu, Kris PT, Cheng, Shirley SW, Ng, Phoebe PY, Mok, Myth TS, Hau, Edgar WL, Lo, Ivan FM

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Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome von Tong, Tony M F, Hau, Edgar W L, Lo, Ivan F M, Chan, Daniel H C, Lam, Stephen T S

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Prader–Willi Syndrome: 16-Year Experience in Hong Kong von Lo, Ivan F.M., Luk, Ho Ming, Tong, Tony M.F., Lai, Kent K.S., Chan, Daniel H.C., Lam, Albert C.F., Chan, David K.H., Hau, Edgar W.L., Fung, Connie O.Y., Lam, Stephen T.S.

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