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H W Ma

Showing results (11-20 of 31) with videos related to

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Clinical and Experimental Obstetrics & Gynecology|June 28, 2018
Successful management of primary splenic pregnancy: a case report and review of literatureB Lv, S T Zhou, H L Peng, et al.
Human Genetics|August 1, 1996
Possible genetic heterogeneity in the Saethre-Chotzen syndromeH W Ma, E Lajeunie, N de Parseval, et al.
Organic Letters|August 25, 2005
Radical-mediated diastereoselective construction of a chiral synthon for synthesis of dolabellanesQ Zhu, K Y Fan, H W Ma, et al.
Genetics and Molecular Research : GMR|October 20, 2012
Novel and recurrent COL2A1 mutations in Chinese patients with spondyloepiphyseal dysplasiaL H Cao, L Wang, C Y Ji, et al.
Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
The Journal of International Medical Research|June 16, 2011
A method of utrophin up-regulation through RNAi-mediated knockdown of the transcription factor EN1Q Wang, D-H Cao, C-L Jin, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|March 4, 1999
Rheologic determinant changes of erythrocytes in Binswanger's diseaseC F Chen, H Y Jia, H W Ma, et al.
The Journal of Biological Chemistry|September 25, 1993
Receptor-evoked Cl- current in Xenopus oocytes is mediated through a beta-type phospholipase C. Cloning of a new form of the enzymeH W Ma, R D Blitzer, E C Healy, et al.
Genetics and Molecular Research : GMR|June 7, 2011
Identification of novel and recurrent mutations in the calcium binding type III repeats of cartilage oligomeric matrix protein in patients with pseudoachondroplasiaL H Cao, L B Wang, S S Wang, et al.
Human Genetics|December 1, 1995
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosisH W Ma, E Lajeunie, M Le Merrer, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Clinical and Experimental Obstetrics & Gynecology|June 28, 2018
Successful management of primary splenic pregnancy: a case report and review of literatureB Lv, S T Zhou, H L Peng, et al.
Human Genetics|August 1, 1996
Possible genetic heterogeneity in the Saethre-Chotzen syndromeH W Ma, E Lajeunie, N de Parseval, et al.
Organic Letters|August 25, 2005
Radical-mediated diastereoselective construction of a chiral synthon for synthesis of dolabellanesQ Zhu, K Y Fan, H W Ma, et al.
Genetics and Molecular Research : GMR|October 20, 2012
Novel and recurrent COL2A1 mutations in Chinese patients with spondyloepiphyseal dysplasiaL H Cao, L Wang, C Y Ji, et al.
Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
The Journal of International Medical Research|June 16, 2011
A method of utrophin up-regulation through RNAi-mediated knockdown of the transcription factor EN1Q Wang, D-H Cao, C-L Jin, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|March 4, 1999
Rheologic determinant changes of erythrocytes in Binswanger's diseaseC F Chen, H Y Jia, H W Ma, et al.
The Journal of Biological Chemistry|September 25, 1993
Receptor-evoked Cl- current in Xenopus oocytes is mediated through a beta-type phospholipase C. Cloning of a new form of the enzymeH W Ma, R D Blitzer, E C Healy, et al.
Genetics and Molecular Research : GMR|June 7, 2011
Identification of novel and recurrent mutations in the calcium binding type III repeats of cartilage oligomeric matrix protein in patients with pseudoachondroplasiaL H Cao, L B Wang, S S Wang, et al.
Human Genetics|December 1, 1995
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosisH W Ma, E Lajeunie, M Le Merrer, et al.
Pageof 4