Search research articles
Contact Us
Filters
Showing results (121-130 of 148) with videos related to
Page
of 15
Sort By:
Clinical and Experimental Dermatology
|
January 9, 2010
One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex
H Y Tang, W D Du, Y Cui, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 28, 2009
Novel missense mutation of keratin in Chinese family with steatocystoma multiplex
J-F Wang, W-S Lu, L-D Sun, et al.
Prenatal Diagnosis
|
August 31, 2006
Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T> A and 79G >T in RMRPgene
Albert C F Lam, Daniel H C Chan, Tony M F Tong, et al.
Forensic Science International
|
March 26, 2018
Evaluation of three rapid oral fluid test devices on the screening of multiple drugs of abuse including ketamine
Magdalene H Y Tang, C K Ching, Simon Poon, et al.
Fetal Diagnosis and Therapy
|
September 30, 2009
Monozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3
W C Leung, H Choi, W L Lau, et al.
ANZ Journal of Surgery
|
February 24, 2025
Needs assessment of surgical skills of interns: a qualitative study in metropolitan Melbourne, Australia
Matthew Y Wei, Howard H Y Tang, Debra Nestel, et al.
Prenatal Diagnosis
|
November 27, 2004
Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong
K Y Leung, C P Lee, M H Y Tang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 7, 2009
Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong
Paulina P Y Ng, Mary H Y Tang, Elizabeth T Lau, et al.
European Journal of Medical Genetics
|
October 16, 2012
A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - is cardiac assessment necessary for all patients with 17p13.3 microduplication?
Alvin C C Ho, Anthony P Y Liu, K S Lun, et al.
Clinical and Experimental Dermatology
|
June 12, 2012
A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family
W Wang, L H Liu, G Chen, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 148) with videos related to
Sort By:
Page
of 15
Clinical and Experimental Dermatology
|
January 9, 2010
One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex
H Y Tang, W D Du, Y Cui, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 28, 2009
Novel missense mutation of keratin in Chinese family with steatocystoma multiplex
J-F Wang, W-S Lu, L-D Sun, et al.
Prenatal Diagnosis
|
August 31, 2006
Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T> A and 79G >T in RMRPgene
Albert C F Lam, Daniel H C Chan, Tony M F Tong, et al.
Forensic Science International
|
March 26, 2018
Evaluation of three rapid oral fluid test devices on the screening of multiple drugs of abuse including ketamine
Magdalene H Y Tang, C K Ching, Simon Poon, et al.
Fetal Diagnosis and Therapy
|
September 30, 2009
Monozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3
W C Leung, H Choi, W L Lau, et al.
ANZ Journal of Surgery
|
February 24, 2025
Needs assessment of surgical skills of interns: a qualitative study in metropolitan Melbourne, Australia
Matthew Y Wei, Howard H Y Tang, Debra Nestel, et al.
Prenatal Diagnosis
|
November 27, 2004
Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong
K Y Leung, C P Lee, M H Y Tang, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|
February 7, 2009
Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong
Paulina P Y Ng, Mary H Y Tang, Elizabeth T Lau, et al.
European Journal of Medical Genetics
|
October 16, 2012
A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - is cardiac assessment necessary for all patients with 17p13.3 microduplication?
Alvin C C Ho, Anthony P Y Liu, K S Lun, et al.
Clinical and Experimental Dermatology
|
June 12, 2012
A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family
W Wang, L H Liu, G Chen, et al.
Page
of 15