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Bai-Lin Wu

Showing results (11-20 of 77) with videos related to

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Current Protocols in Human Genetics|July 13, 2012
Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity statusDavid T Miller, Yiping Shen, Bai-Lin Wu
Clinical Chemistry|October 16, 2012
Exome and whole-genome sequencing as clinical tests: a transformative practice in molecular diagnosticsYongguo Yu, Bai-lin Wu, Jie Wu, et al.
The Journal of Biological Chemistry|November 1, 2003
High intensity ras signaling induces premature senescence by activating p38 pathway in primary human fibroblastsQingdong Deng, Rong Liao, Bai-Lin Wu, et al.
The New England Journal of Medicine|March 7, 2014
Mutations in HFM1 in recessive primary ovarian insufficiencyJian Wang, Wenxiang Zhang, Hong Jiang, et al.
American Journal of Medical Genetics. Part A|August 12, 2003
Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafnessBai-Lin Wu, Margaret Kenna, Va Lip, et al.
Genetic Testing|March 6, 2004
Comparison of PCR-RFLP with allele-specific PCR in genetic testing for spinal muscular atrophyRuliang Xu, Shuji Ogino, Va Lip, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Atypical cases of Angelman syndromeAmy Lawson-Yuen, Bai-Lin Wu, Va Lip, et al.
Science China. Life Sciences|March 18, 2017
Association analysis between HFM1 variations and idiopathic azoospermia or severe oligozoospermia in Chinese MenWenxiang Zhang, Xiaomin Song, Feng Ni, et al.
Science China. Life Sciences|September 4, 2015
Parenting stress and affective symptoms in parents of autistic childrenYun Gong, YaSong Du, HuiLin Li, et al.
Clinical Chemistry|March 28, 2009
Genetic testing for developmental delay: keep searching for an answerDavid T Miller, Yiping Shen, David J Harris, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
Current Protocols in Human Genetics|July 13, 2012
Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity statusDavid T Miller, Yiping Shen, Bai-Lin Wu
Clinical Chemistry|October 16, 2012
Exome and whole-genome sequencing as clinical tests: a transformative practice in molecular diagnosticsYongguo Yu, Bai-lin Wu, Jie Wu, et al.
The Journal of Biological Chemistry|November 1, 2003
High intensity ras signaling induces premature senescence by activating p38 pathway in primary human fibroblastsQingdong Deng, Rong Liao, Bai-Lin Wu, et al.
The New England Journal of Medicine|March 7, 2014
Mutations in HFM1 in recessive primary ovarian insufficiencyJian Wang, Wenxiang Zhang, Hong Jiang, et al.
American Journal of Medical Genetics. Part A|August 12, 2003
Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafnessBai-Lin Wu, Margaret Kenna, Va Lip, et al.
Genetic Testing|March 6, 2004
Comparison of PCR-RFLP with allele-specific PCR in genetic testing for spinal muscular atrophyRuliang Xu, Shuji Ogino, Va Lip, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Atypical cases of Angelman syndromeAmy Lawson-Yuen, Bai-Lin Wu, Va Lip, et al.
Science China. Life Sciences|March 18, 2017
Association analysis between HFM1 variations and idiopathic azoospermia or severe oligozoospermia in Chinese MenWenxiang Zhang, Xiaomin Song, Feng Ni, et al.
Science China. Life Sciences|September 4, 2015
Parenting stress and affective symptoms in parents of autistic childrenYun Gong, YaSong Du, HuiLin Li, et al.
Clinical Chemistry|March 28, 2009
Genetic testing for developmental delay: keep searching for an answerDavid T Miller, Yiping Shen, David J Harris, et al.
Pageof 8