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Cuiping Hou

Showing results (11-20 of 78) with videos related to

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Nucleic Acids Research|September 12, 2008
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platformsSharon J Diskin, Mingyao Li, Cuiping Hou, et al.
Human Heredity|May 4, 2007
DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the geneJubao Duan, Maria Martinez, Alan R Sanders, et al.
Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.
JCI Insight|November 14, 2024
Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1BDong Li, Suzanne Jan de Beur, Cuiping Hou, et al.
Human Mutation|February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey GenocopyPatrick M A Sleiman, Michael March, Kenny Nguyen, et al.
Molecular Autism|April 20, 2013
Whole-genome sequencing in an autism multiplex familyLingling Shi, Xu Zhang, Ryan Golhar, et al.
Journal of Medical Genetics|September 30, 2018
Common variants at 5q33.1 predispose to migraine in African-American childrenXiao Chang, Renata Pellegrino, James Garifallou, et al.
Journal of the National Cancer Institute|February 8, 2022
Identification of Mitochondrial DNA Variants Associated With Risk of NeuroblastomaXiao Chang, Yichuan Liu, Joseph Glessner, et al.
Plos One|April 18, 2015
Genome-wide association study of serum minerals levels in children of different ethnic backgroundXiao Chang, Jin Li, Yiran Guo, et al.
Genes|January 21, 2023
Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood SamplesHui-Qi Qu, Charlly Kao, James Garifallou, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|September 12, 2008
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platformsSharon J Diskin, Mingyao Li, Cuiping Hou, et al.
Human Heredity|May 4, 2007
DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the geneJubao Duan, Maria Martinez, Alan R Sanders, et al.
Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.
JCI Insight|November 14, 2024
Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1BDong Li, Suzanne Jan de Beur, Cuiping Hou, et al.
Human Mutation|February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey GenocopyPatrick M A Sleiman, Michael March, Kenny Nguyen, et al.
Molecular Autism|April 20, 2013
Whole-genome sequencing in an autism multiplex familyLingling Shi, Xu Zhang, Ryan Golhar, et al.
Journal of Medical Genetics|September 30, 2018
Common variants at 5q33.1 predispose to migraine in African-American childrenXiao Chang, Renata Pellegrino, James Garifallou, et al.
Journal of the National Cancer Institute|February 8, 2022
Identification of Mitochondrial DNA Variants Associated With Risk of NeuroblastomaXiao Chang, Yichuan Liu, Joseph Glessner, et al.
Plos One|April 18, 2015
Genome-wide association study of serum minerals levels in children of different ethnic backgroundXiao Chang, Jin Li, Yiran Guo, et al.
Genes|January 21, 2023
Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood SamplesHui-Qi Qu, Charlly Kao, James Garifallou, et al.
Pageof 8