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Journal of Genetic Counseling
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August 15, 2012
Children's acceptance of others with disability: the influence of a disability-simulation program
Christina Hurst, Ken Corning, Richard Ferrante
American Journal of Medical Genetics. Part A
|
January 29, 2011
47, XY, +der(Y),t(X;Y)(p21.1;p11.2): a unique case of XY sex reversal
Yuri A Zarate, Alka Dwivedi, Frank O Bartel, et al.
NPJ Genomic Medicine
|
April 24, 2026
Genetic variants in Rps4x cause intellectual disability with dysmorphic features, microcephaly, and autism
Courtney Matheny-Rabun, Lynda Holloway, Ken Corning, et al.
American Journal of Human Genetics
|
September 9, 2017
RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes
Margot R F Reijnders, Nurhuda M Ansor, Maria Kousi, et al.
Research Square
|
September 18, 2023
Mechanisms of mRNA processing defects in inherited <i>THOC6</i> intellectual disability syndrome
Elizabeth Werren, Geneva LaForce, Anshika Srivastava, et al.
Nature Communications
|
February 22, 2024
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, et al.
Nature Genetics
|
November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Claire Redin, Harrison Brand, Ryan L Collins, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Journal of Genetic Counseling
|
August 15, 2012
Children's acceptance of others with disability: the influence of a disability-simulation program
Christina Hurst, Ken Corning, Richard Ferrante
American Journal of Medical Genetics. Part A
|
January 29, 2011
47, XY, +der(Y),t(X;Y)(p21.1;p11.2): a unique case of XY sex reversal
Yuri A Zarate, Alka Dwivedi, Frank O Bartel, et al.
NPJ Genomic Medicine
|
April 24, 2026
Genetic variants in Rps4x cause intellectual disability with dysmorphic features, microcephaly, and autism
Courtney Matheny-Rabun, Lynda Holloway, Ken Corning, et al.
American Journal of Human Genetics
|
September 9, 2017
RAC1 Missense Mutations in Developmental Disorders with Diverse Phenotypes
Margot R F Reijnders, Nurhuda M Ansor, Maria Kousi, et al.
Research Square
|
September 18, 2023
Mechanisms of mRNA processing defects in inherited <i>THOC6</i> intellectual disability syndrome
Elizabeth Werren, Geneva LaForce, Anshika Srivastava, et al.
Nature Communications
|
February 22, 2024
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava, et al.
Nature Genetics
|
November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Claire Redin, Harrison Brand, Ryan L Collins, et al.
Page
of 1