Hasil Pencarian - Anita Sik Yau Kan

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  1. 1
    Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis

    Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis oleh Mullin Ho Chung Yu, Jeffrey Fong Ting Chau, Sandy Leung Kuen Au, Hei Man Lo, Kit San Yeung, Jasmine Lee Fong Fung, Christopher Chun Yu Mak, Claudia Ching Yan Chung, Kelvin Yuen Kwong Chan, Kelvin Yuen Kwong Chan, Kelvin Yuen Kwong Chan, Brian Hon Yin Chung, Anita Sik Yau Kan, Anita Sik Yau Kan, Anita Sik Yau Kan

    Diterbitkan 2021-01-01
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  2. 2
    Expanded Carrier Screening in Chinese Population – A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women

    Expanded Carrier Screening in Chinese Population – A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women oleh Hiu Yee Heidi Cheng, Grace Ching Yin Wong, Yuen-Kwong Kelvin Chan, Chin Peng Lee, Mary Hoi Yin Tang, Ernest Hung-Yu Ng, Anita Sik-Yau Kan

    Diterbitkan 2020-11-01
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  3. 3
    Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis

    Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis oleh Sheng Mou Lin, Ho Ming Luk, Ivan Fai Man Lo, Wai‐Keung Tam, Kelvin Yuen Kwong Chan, Hei‐Yee Tse, Wing Cheong Leung, Mary Hoi Yin Tang, Anita Sik Yau Kan

    Diterbitkan 2020-08-01
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  4. 4
    A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the <i>OCLN</i> Gene: A Case Report

    A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the <i>OCLN</i> Gene: A Case Report oleh Vivian Kwun Sin Ng, Tze Kin Lau, Anita Sik Yau Kan, Brian Hon Yin Chung, Ho Ming Luk, Wai Fu Ng, Mengmeng Shi, Kwong Wai Choy, Ye Cao, Wing Cheong Leung

    Diterbitkan 2021-08-01
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  5. 5
    Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong

    Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong oleh Claudia Ching Yan Chung, Kelvin Yuen Kwong Chan, Pui Wah Hui, Patrick Kwok Cheung Au, Wai Keung Tam, Samuel Kai Man Li, Gordon Ka Chun Leung, Jasmine Lee Fong Fung, Marcus Chun Yin Chan, Ho Ming Luk, Annisa Shui Lam Mak, Kwok Yin Leung, Mary Hoi Yin Tang, Brian Hon Yin Chung, Anita Sik Yau Kan

    Diterbitkan 2020-02-01
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  6. 6
    Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory

    Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory oleh Theodora Hei Tung Lai, Leung Kuen Sandy Au, Yuen Ting Eunice Lau, Hei Man Lo, Kelvin Yuen Kwong Chan, Ka Wang Cheung, Teresa Wei Ling Ma, Wing Cheong Leung, Choi Wah Kong, Wendy Shu, Po Lam So, Anna Ka Yee Kwong, Christopher Chun Yu Mak, Mianne Lee, Martin Man Chun Chui, Brian Hon Yin Chung, Anita Sik Yau Kan

    Diterbitkan 2022-12-01
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  7. 7
    Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder—implications of a copy number variation involving DPP10

    Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder—implications of a copy number variation involving DPP10 oleh Annisa Shui Lam Mak, Annie Ting Gee Chiu, Gordon Ka Chun Leung, Christopher Chun Yu Mak, Yoyo Wing Yiu Chu, Gary Tsz Kin Mok, Wing Fai Tang, Kelvin Yuen Kwong Chan, Mary Hoi Yin Tang, Elizabeth Tak-Kwong Lau Yim, Kin Wai So, Victoria Qinchen Tao, Cheuk Wing Fung, Virginia Chun Nei Wong, Mohammed Uddin, So Lun Lee, Christian R. Marshall, Stephen W. Scherer, Anita Sik Yau Kan, Brian Hon Yin Chung

    Diterbitkan 2017-06-01
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  8. 8
    Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese

    Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese oleh Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon Yin Chung, Clara Sze Man Tang

    Diterbitkan 2022-03-01
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