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Clinical Chemistry|February 24, 2009
Microarray-based genomic DNA profiling technologies in clinical molecular diagnosticsYiping Shen, Bai-Lin Wu
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
Current Protocols in Human Genetics|July 18, 2008
Oligonucleotide microarrays for clinical diagnosis of copy number variationDavid T Miller, Yiping Shen, Bai-Lin Wu
International Journal of Molecular Sciences|May 7, 2015
Autistic children exhibit decreased levels of essential Fatty acids in red blood cellsSarah A Brigandi, Hong Shao, Steven Y Qian, 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.
Science China. Life Sciences|September 4, 2015
Parenting stress and affective symptoms in parents of autistic childrenYun Gong, YaSong Du, HuiLin Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|September 21, 2011
Age- and gender-dependent obesity in individuals with 16p11.2 deletionYongguo Yu, Haitao Zhu, David T Miller, et al.
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