Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ka Yin Kwok"'
Autor:
Grace Wing Shan Kong, Yanlin Ma, Jian Ou, Yvonne Ka Yin Kwok, Wei Wang, Queenie Sum Yee Yeung, Cherry Kit Man Wong, Qi Li, Wen Xu, Weiying Lu, Hong Li, Tin Chiu Li, Kwong Wai Choy
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 4, Pp 514-520 (2017)
Objective: This study aims to validate the BACs-on-Beads (BoB) technology as a robust and high throughput method for pre-implantation genetic screening (PGS) for aneuploidy. Material and methods: The performances with respect to the sensitivity, spec
Externí odkaz:
https://doaj.org/article/d2bdba40b45f470fa40347a89274e785
Autor:
Pui‐Tak Yu, Wendy Shu, Sau‐Lan Mok, Pui‐Wah Hui, Lin‐Wai Chan, Ka‐Yin Kwok, Kelvin Y. K. Chan, Tsz‐Kin Lo, Brian H. Y. Chung, Ho‐Ming Luk, Anita S. Y. Kan
Publikováno v:
American Journal of Medical Genetics Part A. 188:1562-1567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5805636e983e12a16e6df367c8363157
https://doi.org/10.1002/ajmg.a.62665
https://doi.org/10.1002/ajmg.a.62665
Autor:
Ka Yin Kwok, Rossa W.K. Chiu, Tak Yeung Leung, Wing Cheong Leung, Kwong Wai Choy, Daljit Singh Sahota, Yvonne Kwun Yue Cheng, Tsz-Kin Lo
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 125:451-459
Objective To examine preferences for follow-up testing in women screened with high or intermediate risk for Down syndrome in the first or second trimester. Design Prospective cohort study. Setting Three public hospitals in Hong Kong, China. Sample Wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55bebf387090f8a735fcd23f47883f0c
https://doi.org/10.1111/1471-0528.15022
https://doi.org/10.1111/1471-0528.15022
Publikováno v:
Birth Defects Research. 109:725-733
Chromosome copy number variants (CNVs; gains and losses of DNA sequences >1 kb) are wide-spread throughout the genome of healthy individuals. Laboratory studies show that a subset of CNVs are pathogenic, and not only can be responsible for the pathog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794a5afcddb8d2de46595667ad9eb7fe
https://doi.org/10.1002/bdr2.1054
https://doi.org/10.1002/bdr2.1054
Publikováno v:
Birth defects research. 109(10)
Chromosome copy number variants (CNVs; gains and losses of DNA sequences1 kb) are wide-spread throughout the genome of healthy individuals. Laboratory studies show that a subset of CNVs are pathogenic, and not only can be responsible for the pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c438eb2995ba5f6911302996a9acbca
https://pubmed.ncbi.nlm.nih.gov/28568742
https://pubmed.ncbi.nlm.nih.gov/28568742
Autor:
Peng, Li, Ying, Chen, Xiaoming, Meng, Meng, Xiaoming, Ka Yin, Kwok, Xiaoru, Huang, Kwong Wai, Choy, Chi Chiu, Wang, Huiyao, Lan, Ping, Yuan
Publikováno v:
Stem cell reviews and reports. 9(5)
Disease associated gene deficient embryonic stem cells can serve as valuable in vitro models to study disease mechanisms and screen drugs. Smad3 mediated TGF-β/Activin/Nodal signaling plays important roles in many biological processes. Despite numer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec986fd28a7976a77e6cd58dc1092bdc
https://pubmed.ncbi.nlm.nih.gov/23794057
https://pubmed.ncbi.nlm.nih.gov/23794057
Autor:
Ying, Chen, Jun, Mao, Ka Yin, Kwok, Hui-juan, Kan, Hong-bo, Cheng, Hai-bo, Li, Min-juan, Liu, Ying, Sun, Wen-hua, Yan, Hong, Li, Kwong Wai, Choy
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 27(5)
To establish an assay for screening chromosome 22q11 microdeletion efficiently, and apply it for detecting del22q11 in patients with non-syndromic congenital heart defects (CHD).Seventy nine patients with non-syndromic CHD and 84 normal controls were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::506b68730f3931dcfd255ad6acb1fd9b
https://pubmed.ncbi.nlm.nih.gov/20931540
https://pubmed.ncbi.nlm.nih.gov/20931540
Autor:
Chi Chiu Wang, Ping Yuan, Ying Chen, Peng Li, Xiao-Ru Huang, Ka Yin Kwok, Kwong Wai Choy, Xiao-Ming Meng, Hui-Yao Lan
Publikováno v:
Stem Cell Reviews and Reports. 9:874-874
Disease associated gene deficient embryonic stem cells can serve as valuable in vitro models to study disease mechanisms and screen drugs. Smad3 mediated TGF-β/Activin/Nodal signaling plays important roles in many biological processes. Despite numer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e428608a0be4c13781364ed88a2de17
https://doi.org/10.1007/s12015-013-9475-y
https://doi.org/10.1007/s12015-013-9475-y