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Behavior Genetics
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November 4, 2010
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia
Cecilia Marino, Sara Mascheretti, Valentina Riva, et al.
Journal of Autoimmunity
|
July 30, 2002
Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility
Saijai Cheunsuk, Rachel Sparks, Janice K Noveroske, et al.
American Journal of Human Genetics
|
June 11, 2013
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment
Natalie R Powers, John D Eicher, Falk Butter, et al.
Frontiers in Cell and Developmental Biology
|
August 26, 2022
Dyslexia associated gene <i>KIAA0319</i> regulates cell cycle during human neuroepithelial cell development
Steven Paniagua, Bilal Cakir, Yue Hu, et al.
Genomics
|
October 1, 1992
Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE)
J R Gruen, V L Goei, K M Summers, et al.
Psychosomatic Medicine
|
March 1, 1987
Psychopathology in prenatally DES-exposed females: current and lifetime adjustment
A A Ehrhardt, J F Feldman, L R Rosen, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence
|
August 15, 2019
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes
Miao Li, Dongnhu T Truong, Mellissa DeMille, et al.
Plos One
|
May 22, 2013
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language
John D Eicher, Natalie R Powers, Kelly Cho, et al.
Behavior Genetics
|
November 3, 2010
A dyslexia-associated variant in DCDC2 changes gene expression
Haiying Meng, Natalie R Powers, Ling Tang, et al.
Human Genetics
|
September 1, 2005
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
Haiying Meng, Karl Hager, Matthew Held, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 160) with videos related to
Sort By:
Page
of 16
Behavior Genetics
|
November 4, 2010
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia
Cecilia Marino, Sara Mascheretti, Valentina Riva, et al.
Journal of Autoimmunity
|
July 30, 2002
Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility
Saijai Cheunsuk, Rachel Sparks, Janice K Noveroske, et al.
American Journal of Human Genetics
|
June 11, 2013
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment
Natalie R Powers, John D Eicher, Falk Butter, et al.
Frontiers in Cell and Developmental Biology
|
August 26, 2022
Dyslexia associated gene <i>KIAA0319</i> regulates cell cycle during human neuroepithelial cell development
Steven Paniagua, Bilal Cakir, Yue Hu, et al.
Genomics
|
October 1, 1992
Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE)
J R Gruen, V L Goei, K M Summers, et al.
Psychosomatic Medicine
|
March 1, 1987
Psychopathology in prenatally DES-exposed females: current and lifetime adjustment
A A Ehrhardt, J F Feldman, L R Rosen, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence
|
August 15, 2019
Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes
Miao Li, Dongnhu T Truong, Mellissa DeMille, et al.
Plos One
|
May 22, 2013
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language
John D Eicher, Natalie R Powers, Kelly Cho, et al.
Behavior Genetics
|
November 3, 2010
A dyslexia-associated variant in DCDC2 changes gene expression
Haiying Meng, Natalie R Powers, Ling Tang, et al.
Human Genetics
|
September 1, 2005
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
Haiying Meng, Karl Hager, Matthew Held, et al.
Page
of 16