Search Results - Yu Ming Shiao

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  1. 1
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    Prenatal diagnosis of de novo int22h1/int22h2-mediated Xq28 duplication syndrome involving RAB39B following a previous ambiguous genitalia pregnancy by Yung Chen Chien, Jia Shing Chen, Yu Ming Shiao, Ching Hua Hsiao

    Published 2022
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  2. 2
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    Novel prenatally diagnosed compound heterozygous POMT2 variants in fetal congenital primary aqueduct stenosis by Ju Chin Tsauer, Jia Shing Chen, Yu Ming Shiao, Wei Shin Chou, Yi Fen Chang, Ching Hua Hsiao

    Published 2022
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    Prenatally diagnosed microdeletion in the TCOF1 gene in fetal congenital primary Treacher Collins Syndrome by Wei Shin Chou, Jia Shing Chen, Yu Ming Shiao, Ju Chin Tsauer, Yi Fen Chang, Ching Hua Hsiao

    Published 2022
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    Novel prenatally diagnosed compound heterozygous PXDN variants in fetal congenital primary aphakia and blepharophimosis by Wei Shin Chou, Yu Ming Shiao, Jia Shing Chen, Ju Chin Tsauer, Yi Fen Chang, Yen-Hui Chiu, Ching Hua Hsiao

    Published 2022
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