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R Gruen

Showing results (141-150 of 160) with videos related to

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Human Genetics|August 19, 2016
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disordersD T Truong, L D Shriberg, S D Smith, et al.
American Journal of Medical Genetics. Part A|October 8, 2021
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemiaKelly M Werner, Allison J Cox, Emily Qian, et al.
Psychiatric Genetics|November 20, 2008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sampleKerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, et al.
Human Genetics|February 11, 2014
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQJohn D Eicher, Natalie R Powers, Laura L Miller, et al.
Genomics|August 15, 1996
A transcription map of the major histocompatibility complex (MHC) class I regionJ R Gruen, S R Nalabolu, T W Chu, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2005
DCDC2 is associated with reading disability and modulates neuronal development in the brainHaiying Meng, Shelley D Smith, Karl Hager, et al.
Journal of Medical Genetics|April 19, 2019
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youthDongnhu Thuy Truong, Andrew Kenneth Adams, Steven Paniagua, et al.
Neuropsychology|November 14, 2013
The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING)Natacha Akshoomoff, Erik Newman, Wesley K Thompson, et al.
Current Biology : CB|August 21, 2012
Neuroanatomical assessment of biological maturityTimothy T Brown, Joshua M Kuperman, Yoonho Chung, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2012
Long-term influence of normal variation in neonatal characteristics on human brain developmentKristine B Walhovd, Anders M Fjell, Timothy T Brown, et al.
Pageof 16

Showing results (141-150 of 160) with videos related to

Sort By:
Pageof 16
Human Genetics|August 19, 2016
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disordersD T Truong, L D Shriberg, S D Smith, et al.
American Journal of Medical Genetics. Part A|October 8, 2021
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemiaKelly M Werner, Allison J Cox, Emily Qian, et al.
Psychiatric Genetics|November 20, 2008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sampleKerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, et al.
Human Genetics|February 11, 2014
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQJohn D Eicher, Natalie R Powers, Laura L Miller, et al.
Genomics|August 15, 1996
A transcription map of the major histocompatibility complex (MHC) class I regionJ R Gruen, S R Nalabolu, T W Chu, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2005
DCDC2 is associated with reading disability and modulates neuronal development in the brainHaiying Meng, Shelley D Smith, Karl Hager, et al.
Journal of Medical Genetics|April 19, 2019
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youthDongnhu Thuy Truong, Andrew Kenneth Adams, Steven Paniagua, et al.
Neuropsychology|November 14, 2013
The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING)Natacha Akshoomoff, Erik Newman, Wesley K Thompson, et al.
Current Biology : CB|August 21, 2012
Neuroanatomical assessment of biological maturityTimothy T Brown, Joshua M Kuperman, Yoonho Chung, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2012
Long-term influence of normal variation in neonatal characteristics on human brain developmentKristine B Walhovd, Anders M Fjell, Timothy T Brown, et al.
Pageof 16