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Gynecologic Oncology
|
April 6, 2006
Semi-quantitative fluorescent PCR analysis identifies PRKAA1 on chromosome 5 as a potential candidate cancer gene of cervical cancer
Fung Yu Huang, Pui Man Chiu, Kar Fai Tam, et al.
American Journal of Medical Genetics. Part A
|
July 22, 2014
Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation
K S Yeung, Y Y Chee, H M Luk, et al.
JHEP Reports : Innovation in Hepatology
|
May 3, 2024
Immediate postpartum cessation of tenofovir did not increase risk of virological or clinical relapse in highly viremic pregnant mothers with chronic hepatitis B infection
Yu Chen, Lung-Yi Mak, Mary H Y Tang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 2, 2008
Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: what would be missed, who should decide?
W C Leung, E T Lau, W L Lau, et al.
Hemoglobin
|
September 28, 2017
First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family
Annie S Y Hui, Patrick K C Au, Yuen-Ha Ting, et al.
Plos One
|
April 25, 2013
Noninvasive prenatal molecular karyotyping from maternal plasma
Stephanie C Y Yu, Peiyong Jiang, Kwong W Choy, et al.
Environmental Pollution (Barking, Essex : 1987)
|
June 29, 2026
Association of real-time noise exposure with rest-activity circadian rhythms and sleep health: a 7-day longitudinal measure among Hong Kong nurses with night-shifts
Xueqiong Weng, Natalie H Y Tang, Julie Y T Ma, et al.
Hemoglobin
|
April 1, 2017
An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
Helena H L Lee, Annisa S L Mak, K O Kou, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 28, 2012
Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis
X F Tang, H Y Tang, L D Sun, et al.
Plos One
|
December 15, 2010
Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome
Dana W Y Tsui, Y M Doris Lam, Wing S Lee, et al.
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of 15
Search research articles
Search
Showing results (131-140 of 148) with videos related to
Sort By:
Page
of 15
Gynecologic Oncology
|
April 6, 2006
Semi-quantitative fluorescent PCR analysis identifies PRKAA1 on chromosome 5 as a potential candidate cancer gene of cervical cancer
Fung Yu Huang, Pui Man Chiu, Kar Fai Tam, et al.
American Journal of Medical Genetics. Part A
|
July 22, 2014
Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation
K S Yeung, Y Y Chee, H M Luk, et al.
JHEP Reports : Innovation in Hepatology
|
May 3, 2024
Immediate postpartum cessation of tenofovir did not increase risk of virological or clinical relapse in highly viremic pregnant mothers with chronic hepatitis B infection
Yu Chen, Lung-Yi Mak, Mary H Y Tang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 2, 2008
Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: what would be missed, who should decide?
W C Leung, E T Lau, W L Lau, et al.
Hemoglobin
|
September 28, 2017
First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family
Annie S Y Hui, Patrick K C Au, Yuen-Ha Ting, et al.
Plos One
|
April 25, 2013
Noninvasive prenatal molecular karyotyping from maternal plasma
Stephanie C Y Yu, Peiyong Jiang, Kwong W Choy, et al.
Environmental Pollution (Barking, Essex : 1987)
|
June 29, 2026
Association of real-time noise exposure with rest-activity circadian rhythms and sleep health: a 7-day longitudinal measure among Hong Kong nurses with night-shifts
Xueqiong Weng, Natalie H Y Tang, Julie Y T Ma, et al.
Hemoglobin
|
April 1, 2017
An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
Helena H L Lee, Annisa S L Mak, K O Kou, et al.
Journal of Investigational Allergology & Clinical Immunology
|
March 28, 2012
Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis
X F Tang, H Y Tang, L D Sun, et al.
Plos One
|
December 15, 2010
Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome
Dana W Y Tsui, Y M Doris Lam, Wing S Lee, et al.
Page
of 15