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American Journal of Human Genetics
|
August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype
Michael S Breen, Paras Garg, Lara Tang, et al.
Cells
|
September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> Premutation
Flora Tassone, Dragana Protic, Emily Graves Allen, et al.
Circulation. Cardiovascular Genetics
|
October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3
Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
American Journal of Human Genetics
|
December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Yingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Nature Medicine
|
March 30, 2026
Deleterious coding variation associated with autism is shared across ancestries
Marina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations
Marina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Nature Genetics
|
August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Page
of 35
Search research articles
Search
Showing results (341-350 of 348) with videos related to
Sort By:
Page
of 35
You have reached the last page of results.
This site can display upto 348 results.
American Journal of Human Genetics
|
August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype
Michael S Breen, Paras Garg, Lara Tang, et al.
Cells
|
September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> Premutation
Flora Tassone, Dragana Protic, Emily Graves Allen, et al.
Circulation. Cardiovascular Genetics
|
October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3
Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
American Journal of Human Genetics
|
December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Yingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Nature Medicine
|
March 30, 2026
Deleterious coding variation associated with autism is shared across ancestries
Marina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations
Marina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Nature Genetics
|
August 18, 2022
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack M Fu, F Kyle Satterstrom, Minshi Peng, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Page
of 35