Intellectual Functioning of Children With Isolated PRS, PRS-Plus, and Syndromic PRS von Malarbi, Stephanie, Chisholm, Anita K., Gunn-Charlton, Julia K., Burnett, Alice C., Tan, Tiong Yang, Cheng, Shirley S. W., Pellicano, Anastasia, Shand, Jocelyn, Heggie, Andrew, Hunt, Rod W.

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Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers von Ho, Stephanie K. L., Ng, Samuel Y. L., Yung, Tsz‐Kwai, Mok, Myth T. S., Yiu, Wing‐Chung, Cheng, Heidi H. Y., Cheng, Shirley S. W., Luk, Ho‐ming, Lo, Ivan F. M., Kan, Anita S. Y.

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Adult Chinese twins with Kenny–Caffey syndrome type 2: A potential age‐dependent phenotype and review of literature von Cheng, Shirley S. W., Chan, Pui Kwan Joyce, Luk, Ho‐Ming, Mok, Myth Tsz‐Shun, Lo, Ivan F. M.

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An adult Chinese patient with developmental delay with short stature, dysmorphic features, and sparse hair (Loucks‐Innes syndrome) von Cheng, Shirley S. W., Luk, Ho‐Ming, 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 and phenotype in 18 Chinese patients with Coffin‐Siris syndrome von Cheng, Shirley S. W., Luk, Ho‐Ming, Mok, Myth Tsz‐Shun, Leung, Sha‐Sha, Lo, Ivan F. M.

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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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First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing von Shu, Wendy, Cheng, Shirley S W, Xue, Shuwen, Chan, Lin Wai, Soong, Sung Inda, Kan, Anita Sik Yau, Cheung, Sunny Wai Hung, Choy, Kwong Wai

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CHARGE syndrome in nine patients from China von Cheng, Shirley S. W., Luk, Ho‐Ming, Chan, David K. H., Lo, Ivan F. M.

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Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders von Cao, Ye, Luk, Ho Ming, Zhang, Yanyan, Chau, Matthew Hoi Kin, Xue, Shuwen, Cheng, Shirley S W, Li, Albert Martin, Chong, Josephine S C, Leung, Tak Yeung, Dong, Zirui, Choy, Kwong Wai, Lo, Ivan Fai Man

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