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Bai-Lin Wu

Showing results (41-50 of 77) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2002
Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testingBai-Lin Wu, Neal Lindeman, Va Lip, et al.
Frontiers in Cardiovascular Medicine|January 28, 2025
Cardiac computer tomography-derived radiomics in assessing myocardial characteristics at the connection between the left atrial appendage and the left atrium in atrial fibrillation patientsXiao-Xuan Wei, Cai-Ying Li, Hai-Qing Yang, et al.
Journal of Magnetic Resonance Imaging : JMRI|March 27, 2016
Quantitative evaluation of left ventricular volume and function in middle-aged healthy chinese people with 3 Tesla MRICai-Ying Li, Bu-Lang Gao, Fu-Qian Guo, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control studyXiaoli Chen, Jin Guo, Yunping Lei, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese familyYiping Shen, Xiaoli Chen, Liwen Wang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|January 18, 2006
[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients]Pu Dai, Fei Yu, Dong-yang Kang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|February 5, 2021
A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertilityWen-Bin He, Ya-Xin Zhang, Chen Tan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 20, 2021
LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant miceLi Yu, Lina Wang, Wufan Tao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalitiesHeather Mason-Suares, Wayne Kim, Leslie Grimmett, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2002
Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testingBai-Lin Wu, Neal Lindeman, Va Lip, et al.
Frontiers in Cardiovascular Medicine|January 28, 2025
Cardiac computer tomography-derived radiomics in assessing myocardial characteristics at the connection between the left atrial appendage and the left atrium in atrial fibrillation patientsXiao-Xuan Wei, Cai-Ying Li, Hai-Qing Yang, et al.
Journal of Magnetic Resonance Imaging : JMRI|March 27, 2016
Quantitative evaluation of left ventricular volume and function in middle-aged healthy chinese people with 3 Tesla MRICai-Ying Li, Bu-Lang Gao, Fu-Qian Guo, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control studyXiaoli Chen, Jin Guo, Yunping Lei, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese familyYiping Shen, Xiaoli Chen, Liwen Wang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|January 18, 2006
[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients]Pu Dai, Fei Yu, Dong-yang Kang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|February 5, 2021
A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertilityWen-Bin He, Ya-Xin Zhang, Chen Tan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 20, 2021
LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant miceLi Yu, Lina Wang, Wufan Tao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalitiesHeather Mason-Suares, Wayne Kim, Leslie Grimmett, et al.
Pageof 8