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Nucleic Acids Research
|
September 12, 2008
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
Sharon 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 gene
Jubao 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 dysmorphism
Dong 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 1B
Dong Li, Suzanne Jan de Beur, Cuiping Hou, et al.
Human Mutation
|
February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy
Patrick M A Sleiman, Michael March, Kenny Nguyen, et al.
Molecular Autism
|
April 20, 2013
Whole-genome sequencing in an autism multiplex family
Lingling 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 children
Xiao 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 Neuroblastoma
Xiao 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 background
Xiao 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 Samples
Hui-Qi Qu, Charlly Kao, James Garifallou, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 78) with videos related to
Sort By:
Page
of 8
Nucleic Acids Research
|
September 12, 2008
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
Sharon 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 gene
Jubao 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 dysmorphism
Dong 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 1B
Dong Li, Suzanne Jan de Beur, Cuiping Hou, et al.
Human Mutation
|
February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy
Patrick M A Sleiman, Michael March, Kenny Nguyen, et al.
Molecular Autism
|
April 20, 2013
Whole-genome sequencing in an autism multiplex family
Lingling 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 children
Xiao 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 Neuroblastoma
Xiao 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 background
Xiao 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 Samples
Hui-Qi Qu, Charlly Kao, James Garifallou, et al.
Page
of 8