Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Wendy Shu"'
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
Autor:
Linus LT Lee, Wendy Shu
Publikováno v:
Hong Kong Journal of Gynaecology, Obstetrics and Midwifery. 22:16-20
Autor:
Wendy Shu
Publikováno v:
Journal of Obstetrics and Gynaecology Canada. 43:1274-1278
Objective To evaluate the diagnostic value of the “sliding sign”, a sonographic test, in predicting intra-abdominal adhesions for women undergoing repeat cesarean delivery. Methods This was a prospective observational study of women undergoing a
Autor:
Po Lam So, Annie Shuk Yi Hui, Teresa Wei Ling Ma, Wendy Shu, Amelia Pui Wah Hui, Choi Wah Kong, Tsz Kin Lo, Amanda Nim Chi Kan, Elaine Yee Ling Kan, Shuk Ching Chong, Brian Hon Yin Chung, Ho Ming Luk, Kwong Wai Choy, Anita Sik Yau Kan, Wing Cheong Leung
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 2088
With the advancements in prenatal diagnostics, genome sequencing is now incorporated into clinical use to maximize the diagnostic yield following uninformative conventional tests (karyotype and chromosomal microarray analysis). Hong Kong started publ
Autor:
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
Publikováno v:
Healthcare; Volume 10; Issue 12; Pages: 2521
Fetal structural congenital abnormalities (SCAs) complicate 2–3% of all pregnancies. Whole-exome sequencing (WES) has been increasingly adopted prenatally when karyotyping and chromosomal microarray do not yield a diagnosis. This is a retrospective
Autor:
Sung Inda Soong, Lin Wai Chan, Anita Sik Yau Kan, Sunny Wai Hung Cheung, Wendy Shu, Shuwen Xue, Shirley S. W. Cheng, Kwong Wai Choy
Publikováno v:
Genes
Genes, Vol 12, Iss 370, p 370 (2021)
Volume 12
Issue 3
Genes, Vol 12, Iss 370, p 370 (2021)
Volume 12
Issue 3
Tetrasomy 9p (ORPHA:3390) is a rare syndrome, hallmarked by growth retardation
psychomotor delay
mild to moderate intellectual disability
and a spectrum of skeletal, cardiac, renal and urogenital defects. Here we present a Chinese fema
psychomotor delay
mild to moderate intellectual disability
and a spectrum of skeletal, cardiac, renal and urogenital defects. Here we present a Chinese fema
Autor:
Hei-Man TAM, Wendy SHU
Publikováno v:
Hong Kong Journal of Gynaecology, Obstetrics & Midwifery; Jul2022, Vol. 22 Issue 2, p81-86, 6p
Publikováno v:
Humanities & Social Sciences Communications, Vol 10, Iss 1, Pp 1-8 (2023)
Abstract Authors used an andragogy framework to help undergraduate allied health students better understand social determinants of health (SDOH) using a photo essay assignment. The study examined students’ perceptions of SDOH in various communities
Externí odkaz:
https://doaj.org/article/b4b217b86ff6406fbd161e7be62eb01d
Publikováno v:
Hong Kong Medical Journal. :636-636
Publikováno v:
Biotechnology and Bioengineering. 54:231-238
As part of the program to scale-up the production of artificial seeds of winter oilseed rape, Brassica napus ssp. oleifera, we established a liquid flask culture system that enables the high frequency production of freely suspended embryos. As many a