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Electrophoresis
|
August 10, 2004
Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis
Lee-Jun C Wong, Tian-Jian Chen, Duan-Jun Tan
Pediatric Research
|
April 1, 2021
Cytogenomic aberrations in isolated multicystic dysplastic kidney in children
Tian-Jian Chen, Renfang Song, Adam Janssen, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
August 19, 2006
Molecular analysis of mitochondrial DNA point mutations by polymerase chain reaction
Lee-Jun C Wong, Bryan R Cobb, Tian-Jian Chen
Clinical Dysmorphology
|
April 12, 2014
Duplication at Xq28 involving IKBKG is associated with progressive macrocephaly, recurrent infections, ectodermal dysplasia, benign tumors, and neuropathy
Ellyze van Asbeck, Arivudainambi Ramalingam, Chris Dvorak, et al.
Behavioral and Brain Functions : BBF
|
May 1, 2008
Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations
Xiaozhu Wang, Zheng Wang, Ming Yan, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Development of a molecular screening test for hereditary hearing loss and genetic susceptibility to aminoglycoside toxicity for Chinese population
Xi-yu He, Yue-ying Wang, Pu Dai, et al.
Muscle & Nerve
|
July 1, 2006
Exercise intolerance associated with a novel 8300T > C mutation in mitochondrial transfer RNAlys
Michael J Gambello, Ren-Kui Bai, Tian-Jian Chen, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Constitutional mosaic trisomy 21 and azoospermia: a case report
Guo-hui Lu, Janice G Edwards, Gail Whitman-Elia, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2004
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation
Andrea Gropman, Tian-Jian Chen, Cherng-Lih Perng, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome
Yueying Wang, Jose E Martinez, Glen L Wilson, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Electrophoresis
|
August 10, 2004
Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis
Lee-Jun C Wong, Tian-Jian Chen, Duan-Jun Tan
Pediatric Research
|
April 1, 2021
Cytogenomic aberrations in isolated multicystic dysplastic kidney in children
Tian-Jian Chen, Renfang Song, Adam Janssen, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
August 19, 2006
Molecular analysis of mitochondrial DNA point mutations by polymerase chain reaction
Lee-Jun C Wong, Bryan R Cobb, Tian-Jian Chen
Clinical Dysmorphology
|
April 12, 2014
Duplication at Xq28 involving IKBKG is associated with progressive macrocephaly, recurrent infections, ectodermal dysplasia, benign tumors, and neuropathy
Ellyze van Asbeck, Arivudainambi Ramalingam, Chris Dvorak, et al.
Behavioral and Brain Functions : BBF
|
May 1, 2008
Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations
Xiaozhu Wang, Zheng Wang, Ming Yan, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Development of a molecular screening test for hereditary hearing loss and genetic susceptibility to aminoglycoside toxicity for Chinese population
Xi-yu He, Yue-ying Wang, Pu Dai, et al.
Muscle & Nerve
|
July 1, 2006
Exercise intolerance associated with a novel 8300T > C mutation in mitochondrial transfer RNAlys
Michael J Gambello, Ren-Kui Bai, Tian-Jian Chen, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences
|
February 19, 2005
Constitutional mosaic trisomy 21 and azoospermia: a case report
Guo-hui Lu, Janice G Edwards, Gail Whitman-Elia, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2004
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation
Andrea Gropman, Tian-Jian Chen, Cherng-Lih Perng, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome
Yueying Wang, Jose E Martinez, Glen L Wilson, et al.
Page
of 2