Search Results - Cheng, Wai-Fun

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  1. 1
    The physical and developmental outcomes of children whose mothers are substance abusers: Analysis of associated factors and the impact of early intervention

    The physical and developmental outcomes of children whose mothers are substance abusers: Analysis of associated factors and the impact of early intervention by Cheng, Anna Wai Fun, Chan, Hin Biu, Ip, Lai Sheung, Wan, Katy Kit Ying, Yu, Ellen Lok Man, Chiu, Wa Keung, Chung, Pui Hong, Yeoh, Eng Kiong

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  2. 2
    Second malignant neoplasms in childhood cancer survivors in a tertiary paediatric oncology centre in Hong Kong, China

    Second malignant neoplasms in childhood cancer survivors in a tertiary paediatric oncology centre in Hong Kong, China by Sun, Wai-Fun, Cheng, Frankie Wai-Tsoi, Lee, Vincent, Leung, Wing-Kwan, Shing, Ming-Kong, Yuen, Patrick Man-Pan, Li, Chi-Kong

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  3. 3
    Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome

    Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome by Lam, Ching-Wan, Yuen, Yuet-Ping, Cheng, Wai-Fun, Chan, Yan-Wo, Tong, Sui-Fan

    Published in Clinica chimica acta
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  4. 4
    Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b

    Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b by Yuen, Yuet-Ping, Cheng, Wai-Fun, Tong, Sui-Fan, Chan, Yuk-Tat, Chan, Yan-Wo, Lam, Ching-Wan

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  5. 5
    Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia

    Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia by Lam, Ching-Wan, Cheng, Anna Wai-Fun, Poon, Wing-Tat, Yuen, Yuet-Ping, Huen, Kwai-Fun

    Published in Clinica chimica acta
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  6. 6
    Novel Donor Splice Site Mutation of ABCG5 Gene in Sitosterolemia

    Novel Donor Splice Site Mutation of ABCG5 Gene in Sitosterolemia by Lam, Ching-Wan, Cheng, Anna Wai-Fun, Tong, Sui-Fan, Chan, Yan-Wo

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  7. 7
    DNA-Based Diagnosis of Isolated Sulfite Oxidase Deficiency by Denaturing High-Performance Liquid Chromatography

    DNA-Based Diagnosis of Isolated Sulfite Oxidase Deficiency by Denaturing High-Performance Liquid Chromatography by Lam, Ching-Wan, Li, Chi-Keung, Lai, Chi-Kong, Tong, Sui-Fan, Chan, Kwok-Yin, Ng, Grace Sui-Fun, Yuen, Yuet-Ping, Cheng, Anna Wai-Fun, Chan, Yan-Wo

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  8. 8
    WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b

    WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b by Yuen, Yuet-Ping, Cheng, Wai-Fun, Tong, Sui-Fan, Chan, Yuk-Tat, Chan, Yan-Wo, Lam, Ching-Wan

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  9. 9
    WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b

    WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b by Yuen, Yuet-Ping, Cheng, Wai-Fun, Tong, Sui-Fan, Chan, Yuk-Tat, Chan, Yan-Wo, Lam, Ching-Wan

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