Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Mary Hoi Yin Tang"'
Autor:
Lu Hong, Mary Hoi Yin Tang, Ka Wang Cheung, Libing Luo, Cindy Ka Yee Cheung, Xiaoying Dai, Yanyan Li, Chuqin Xiong, Wei Liang, Wei Xiang, Liangbing Wang, Kelvin Yuen Kwong Chan, Shengmou Lin
Publikováno v:
Diagnostics, Vol 14, Iss 1, p 102 (2024)
Fetal hyperthyroidism can occur secondary to maternal autoimmune hyperthyroidism. The thyroid-stimulating hormone receptor antibody (TRAb) transferred from the mother to the fetus stimulates the fetal thyroid and causes fetal thyrotoxicosis. Fetuses
Externí odkaz:
https://doaj.org/article/5392aa4c38ad41fcb38ee13259183e38
Autor:
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
Publikováno v:
Clinical Case Reports, Vol 8, Iss 8, Pp 1369-1375 (2020)
Abstract Mosaic variegated aneuploidy (MVA) is a rare genetic disorder caused by mutations in BUB1B, CEP57, or TRIP13. We describe the prenatal diagnosis, molecular characterization, and clinical management of a long‐lived patient with BUB1B‐rela
Externí odkaz:
https://doaj.org/article/5f7d3ec0503c48448b3030a1433f610f
Autor:
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
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-15 (2020)
Abstract Background Chromosomal microarray (CMA) has been shown to be cost-effective over karyotyping in invasive prenatal diagnosis for pregnancies with fetal ultrasound anomalies. Yet, information regarding preceding and subsequent tests must be co
Externí odkaz:
https://doaj.org/article/5b55676ef2a14980ab6727835e25d33b
Autor:
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
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
ObjectiveRecessive genetic diseases impose physical and psychological impacts to both newborns and parents who may not be aware of being carriers. Expanded carrier screening (ECS) allows screening for multiple genetic conditions at the same time. Whe
Externí odkaz:
https://doaj.org/article/91482c9680dd4eecb59ccd867e333f40
Autor:
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
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-12 (2017)
Abstract Background Array comparative genomic hybridization (aCGH) is recommended as a first-tier genetic test for children with autism spectrum disorder (ASD). However, interpretation of results can often be challenging partly due to the fact that c
Externí odkaz:
https://doaj.org/article/f4d95ed70644412987ce07feaa2f58c6
Autor:
Ivan F M Lo, Anita Sik Yau Kan, Hei‐Yee Tse, Wai-Keung Tam, Kelvin Y.K. Chan, Wing Cheong Leung, Ho Ming Luk, Sheng Mou Lin, Mary Hoi Yin Tang
Publikováno v:
Clinical Case Reports, Vol 8, Iss 8, Pp 1369-1375 (2020)
Clinical Case Reports
Clinical Case Reports
Mosaic variegated aneuploidy (MVA) is a rare genetic disorder caused by mutations in BUB1B, CEP57, or TRIP13. We describe the prenatal diagnosis, molecular characterization, and clinical management of a long‐lived patient with BUB1B‐related MVA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::901c647833b647e03182eef8ae970333
https://doaj.org/article/5f7d3ec0503c48448b3030a1433f610f
https://doaj.org/article/5f7d3ec0503c48448b3030a1433f610f
Autor:
Annisa S. L. Mak, Teresa W. L. Ma, Kwok Y. Leung, Kelvin Y.K. Chan, Mary Hoi Yin Tang, Anita Sik Yau Kan
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 45:923-926
It is difficult to prenatally identify 5p deletion (-) syndrome. Here, we report five cases of 5p- syndrome diagnosed by invasive prenatal diagnosis. Of them, three had a small cerebellum in the second trimester. In one case, a prominent renal pelvis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a4c6054aa3cde39219ae34c76949340
https://doi.org/10.1111/jog.13911
https://doi.org/10.1111/jog.13911
Autor:
Anita Sik Yau Kan, Ernest Hung Yu Ng, Chin Peng Lee, Hiu Yee Heidi Hyh Cheng, Grace Ching Yin Wong, Mary Hoi Yin Tang, Yuen-Kwong Kelvin Chan
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics, Vol 11 (2020)
Objective Recessive genetic diseases impose physical and psychological impacts to both newborns and parents who may not be aware of being carriers. Expanded carrier screening (ECS) allows screening for multiple genetic conditions at the same time. Wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6510f92c6de33885984993b6523de907
http://europepmc.org/articles/PMC7701308
http://europepmc.org/articles/PMC7701308
Autor:
Anthony P. Y. Liu, Jasmine L.F. Fung, Mullin H.C. Yu, Chin Peng Lee, Anita Sik Yau Kan, Wanling Yang, Gary T. K. Mok, Gordon K.C. Leung, Mandy H.Y. Tsang, Amelia P W Hui, Steven L.C. Pei, KS Yeung, Kelvin Y.K. Chan, Pak C. Sham, Wilfred Hing Sang Wong, Brian H.Y. Chung, Mary Hoi Yin Tang, Christopher C.Y. Mak
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-10 (2018)
BMC Medical Genomics
BMC Medical Genomics
Background Whole-exome sequencing (WES) has become an invaluable tool for genetic diagnosis in paediatrics. However, it has not been widely adopted in the prenatal setting. This study evaluated the use of WES in prenatal genetic diagnosis in fetuses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840c691f01fd45f268af6807c2658291
http://link.springer.com/article/10.1186/s12920-018-0409-z
http://link.springer.com/article/10.1186/s12920-018-0409-z
Autor:
Kam Cheong Lee, Mark D. Pertile, Wing Cheuk Wong, Mary Hoi Yin Tang, Chun Hong So, Anita Sik Yau Kan, Wan Pang Chan, Elizabeth T. Lau
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 44:955-959
A complete hydatidiform mole (CHM) coexisting with a viable fetus is a rare finding in pregnancies. Accurate diagnosis often relies on ultrasonographic, histopathological and molecular techniques in the definite diagnosis. To the best of our knowledg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::856531ba51a913d79f0e502931050961
https://doi.org/10.1111/jog.13598
https://doi.org/10.1111/jog.13598