Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Zhong Xi Yi Jie He Za Zhi = Chinese Journal of Modern Developments in Traditional Medicine|February 1, 1991
[Preventive effect of re du qing on hepatocytes and mitochondria damaged by lipid peroxidation in experimental rabbits with endotoxin-induced disseminated intravascular coagulation]Z M Deng, W Y Ye, M Z Li
British Journal of Haematology|January 1, 1994
The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma geneP I Motum, Z M Deng, L Huong, et al.
Human Genetics|April 1, 1994
Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndromeA Smith, Z M Deng, R Beran, et al.
Molecular Vision|November 28, 2001
Altered expression of alternatively spliced isoforms of the mRNA NMDAR1 receptor in the visual cortex of strabismic catsZ Q Yin, Z M Deng, S G Crewther, et al.
The Medical Journal of Australia|June 21, 1993
Novel patterns of inheritance of genetic disease are illustrated by the Angelman syndromeZ M Deng, T Woodage, R Smart, et al.
Disease Markers|March 1, 1996
Establishment of sequence-tagged sites on 15q11-q13 by Alu-vector PCR cloning of YAC-generated fragmentsW S Kim, Z M Deng, N T Nassif, et al.
Archives of Disease in Childhood|May 1, 1995
Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromesA Smith, M Prasad, Z M Deng, et al.
Genomics|January 1, 1994
Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13T Woodage, R Lindeman, Z M Deng, et al.
Clinical Genetics|January 1, 1993
Fluorescence in-situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader-Willi syndromeA Smith, L Robson, A Neumann, et al.
American Journal of Medical Genetics|September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndromeT Woodage, Z M Deng, M Prasad, et al.
Pageof 2