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American Journal of Medical Genetics. Part A
|
September 24, 2004
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10
Satoko Shimizu, Charles Krafchak, Nobuo Fuse, et al.
American Journal of Ophthalmology
|
March 26, 2003
Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy
Sayoko E Moroi, Parag A Gokhale, Miriam T Schteingart, et al.
American Journal of Human Genetics
|
March 5, 2016
A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants
K Alaine Broadaway, David J Cutler, Richard Duncan, et al.
JAMA
|
March 20, 2008
Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults
Elisabeth B Binder, Rebekah G Bradley, Wei Liu, et al.
Molecular Psychiatry
|
April 13, 2019
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
Timothy P Rutkowski, Ryan H Purcell, Rebecca M Pollak, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
December 13, 2021
Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study
Anke Hüls, Catherine J Wedderburn, Nynke A Groenewold, et al.
Human Molecular Genetics
|
April 16, 2019
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk
Hyerim Kim, Junghwa Lim, Han Bao, et al.
HGG Advances
|
April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip
Sarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Archives of General Psychiatry
|
February 6, 2008
Influence of child abuse on adult depression: moderation by the corticotropin-releasing hormone receptor gene
Rebekah G Bradley, Elisabeth B Binder, Michael P Epstein, et al.
Pediatric Rheumatology Online Journal
|
October 29, 2013
Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA
Merlyn J Kaalla, K Alaine Broadaway, Mina Rohani-Pichavant, et al.
Page
of 14
Search research articles
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Showing results (101-110 of 140) with videos related to
Sort By:
Page
of 14
American Journal of Medical Genetics. Part A
|
September 24, 2004
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10
Satoko Shimizu, Charles Krafchak, Nobuo Fuse, et al.
American Journal of Ophthalmology
|
March 26, 2003
Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy
Sayoko E Moroi, Parag A Gokhale, Miriam T Schteingart, et al.
American Journal of Human Genetics
|
March 5, 2016
A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants
K Alaine Broadaway, David J Cutler, Richard Duncan, et al.
JAMA
|
March 20, 2008
Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults
Elisabeth B Binder, Rebekah G Bradley, Wei Liu, et al.
Molecular Psychiatry
|
April 13, 2019
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
Timothy P Rutkowski, Ryan H Purcell, Rebecca M Pollak, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
December 13, 2021
Newborn differential DNA methylation and subcortical brain volumes as early signs of severe neurodevelopmental delay in a South African Birth Cohort Study
Anke Hüls, Catherine J Wedderburn, Nynke A Groenewold, et al.
Human Molecular Genetics
|
April 16, 2019
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk
Hyerim Kim, Junghwa Lim, Han Bao, et al.
HGG Advances
|
April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip
Sarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Archives of General Psychiatry
|
February 6, 2008
Influence of child abuse on adult depression: moderation by the corticotropin-releasing hormone receptor gene
Rebekah G Bradley, Elisabeth B Binder, Michael P Epstein, et al.
Pediatric Rheumatology Online Journal
|
October 29, 2013
Meta-analysis confirms association between TNFA-G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA
Merlyn J Kaalla, K Alaine Broadaway, Mina Rohani-Pichavant, et al.
Page
of 14