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Current Protocols in Human Genetics
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July 13, 2012
Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status
David 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 diagnostics
Yongguo 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 fibroblasts
Qingdong Deng, Rong Liao, Bai-Lin Wu, et al.
The New England Journal of Medicine
|
March 7, 2014
Mutations in HFM1 in recessive primary ovarian insufficiency
Jian 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 deafness
Bai-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 atrophy
Ruliang Xu, Shuji Ogino, Va Lip, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Atypical cases of Angelman syndrome
Amy 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 Men
Wenxiang Zhang, Xiaomin Song, Feng Ni, et al.
Science China. Life Sciences
|
September 4, 2015
Parenting stress and affective symptoms in parents of autistic children
Yun Gong, YaSong Du, HuiLin Li, et al.
Clinical Chemistry
|
March 28, 2009
Genetic testing for developmental delay: keep searching for an answer
David T Miller, Yiping Shen, David J Harris, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 77) with videos related to
Sort By:
Page
of 8
Current Protocols in Human Genetics
|
July 13, 2012
Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status
David 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 diagnostics
Yongguo 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 fibroblasts
Qingdong Deng, Rong Liao, Bai-Lin Wu, et al.
The New England Journal of Medicine
|
March 7, 2014
Mutations in HFM1 in recessive primary ovarian insufficiency
Jian 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 deafness
Bai-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 atrophy
Ruliang Xu, Shuji Ogino, Va Lip, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Atypical cases of Angelman syndrome
Amy 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 Men
Wenxiang Zhang, Xiaomin Song, Feng Ni, et al.
Science China. Life Sciences
|
September 4, 2015
Parenting stress and affective symptoms in parents of autistic children
Yun Gong, YaSong Du, HuiLin Li, et al.
Clinical Chemistry
|
March 28, 2009
Genetic testing for developmental delay: keep searching for an answer
David T Miller, Yiping Shen, David J Harris, et al.
Page
of 8