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Bai-Lin Wu

Showing results (51-60 of 77) with videos related to

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Plos One|April 18, 2012
High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disabilityXiaohong Gong, Yu-Wu Jiang, Xin Zhang, et al.
Plos One|January 26, 2013
Detection of copy number variants reveals association of cilia genes with neural tube defectsXiaoli Chen, Yiping Shen, Yonghui Gao, et al.
Frontiers in Physiology|July 10, 2015
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393WFabian R Reimold, Savithri Balasubramanian, David B Doroquez, et al.
BMC Genetics|October 20, 2009
Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genesRichard R Bennett, Hal E Schneider, Elicia Estrella, et al.
Human Mutation|May 22, 2012
Identification of novel rare mutations of DACT1 in human neural tube defectsYan Shi, Yi Ding, Yun-Ping Lei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
American Journal of Human Genetics|November 29, 2011
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletionsAndrew Dauber, Yongguo Yu, Michael C Turchin, et al.
Human Mutation|December 8, 2016
Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction FormationXiaoli Chen, Yu An, Yonghui Gao, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Plos One|April 18, 2012
High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disabilityXiaohong Gong, Yu-Wu Jiang, Xin Zhang, et al.
Plos One|January 26, 2013
Detection of copy number variants reveals association of cilia genes with neural tube defectsXiaoli Chen, Yiping Shen, Yonghui Gao, et al.
Frontiers in Physiology|July 10, 2015
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393WFabian R Reimold, Savithri Balasubramanian, David B Doroquez, et al.
BMC Genetics|October 20, 2009
Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genesRichard R Bennett, Hal E Schneider, Elicia Estrella, et al.
Human Mutation|May 22, 2012
Identification of novel rare mutations of DACT1 in human neural tube defectsYan Shi, Yi Ding, Yun-Ping Lei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
American Journal of Human Genetics|November 29, 2011
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletionsAndrew Dauber, Yongguo Yu, Michael C Turchin, et al.
Human Mutation|December 8, 2016
Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction FormationXiaoli Chen, Yu An, Yonghui Gao, et al.
Pageof 8