Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Tse Ngong, Leung"'
Autor:
Gavin Chapman, Carla Campagnolo, Josue Flores-Daboub, Ye Cao, Kwong Wai Choy, Tse Ngong Leung, Lauren E. Westerfield, Kavitha R Iyer, Pengfei Liu, Rui Xiao, Victoria Mok Siu, Thomas A. Drysdale, Sally L. Dunwoodie, Weimin Bi, Justin O. Szot, Hartmut Cuny
Publikováno v:
Paediatrics Publications
Am J Hum Genet
Am J Hum Genet
Birth defects occur in up to 3% of all live births and are the leading cause of infant death. Here we present five individuals from four unrelated families, individuals who share similar phenotypes with disease-causal bi-allelic variants in NADSYN1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e1b038ea30dbbf86082aa89929c23e4
https://ir.lib.uwo.ca/paedpub/434
https://ir.lib.uwo.ca/paedpub/434
Publikováno v:
Asia-Oceania Journal of Obstetrics and Gynaecology. 20:173-177
Four babies with congenital listeriosis were diagnosed in the Prince of Wales Hospital in Hong Kong in 1990-1991. Two died in the early neonatal period. The remaining 2 survived and recovered with no sequelae. The clinical and pathological features o
Autor:
Tze Kin Lau, Tse Ngong Leung, Tak Yuen Fung, Lai Wa Law, Lin Wai Chan, Tak Yeung Leung, Daljit Singh Sahota
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 22:300-304
To examine the effectiveness of first trimester fetal Trisomy 21 (T21) screening using a combination of maternal age, nuchal translucency, maternal serum levels of free beta-hCG and PAPP-A in a predominantly Chinese population in Hong Kong.Consecutiv
Autor:
Yuk Ming Dennis Lo, John Wong, Raymond S.M. Wong, Rebecca W.Y. Chan, WK Chan, Yvonne Kwun Yue Cheng, Kun Sun, David S.C. Hui, Simon S.M. Ng, Tse Ngong Leung, Stephen L. Chan, Suk Hang Cheng, Peiyong Jiang, Yu K. Tong, Edmond S. K. Ma, Rossa W.K. Chiu, K.C. Allen Chan, Raymond Liang, Tak Yeung Leung, Paul B.S. Lai
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 112(40)
Plasma consists of DNA released from multiple tissues within the body. Using genome-wide bisulfite sequencing of plasma DNA and deconvolution of the sequencing data with reference to methylation profiles of different tissues, we developed a general a
Autor:
Wing Yee Fok, Tze Kin Lau, Tse Ngong Leung, Tony K.H. Chung, Michelle Hang Yuet Tsui, Louis Yik-Si Chan
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 125:206-210
Objective To evaluate the pregnancy outcomes of two policies of timing of induction of labor for post-term pregnancies. Study design It is a retrospective study in a University obstetric unit from 1997 to 2002. Five thousand eight hundred and ninety-
Publikováno v:
Prenatal Diagnosis. 26:819-824
Objective This study was performed to investigate the preferences of Chinese pregnant women for Down syndrome-affected birth compared to invasive test-related miscarriage, using the standard gamble approach, and to investigate whether there is a diff
Publikováno v:
Fetal Diagnosis and Therapy. 21:140-143
Objective: To study the effect of ethnic Chinese on the medians of free β-hCG and PAPP-A in the first trimester of pregnancy. Methods: The data of 943 women undergoing first trimester combined screening for fetal Down syndrome were analysed to deriv
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 26:713-717
Objective To assess the value of a single cervical length measurement by transvaginal sonography (TVS) at the time of mid-trimester anomaly scan for predicting spontaneous preterm delivery (SPD) among Chinese women. Methods A prospective observationa
Publikováno v:
BJOG: An International Journal of Obstetrics and Gynaecology. 112:1568-1571
In a prospective study of 247 pregnant Chinese women, the prevalence of sleep disturbances across pregnancy has been assessed using a set of validated questionnaires including the Sleep and Health Questionnaire (SHQ) and the Epworth Sleepiness Scale
Autor:
Tse Ngong Leung, Tze Kin Lau
Publikováno v:
Current Opinion in Obstetrics & Gynecology. 17:163-169
The purpose of the review was to review the latest developments in screening and diagnosis of non-chromosomal genetic diseases. Major recent advances include the completion of the Human Genome Project the use of microarray and related technologies fo