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L Ritter

Showing results (281-290 of 287) with videos related to

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Frontiers in Molecular Neuroscience|April 8, 2017
Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD)McKenzie L Ritter, Wei Guo, Jack F Samuels, et al.
American Journal of Human Genetics|October 8, 2019
Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive ImpairmentSarah K Fiordaliso, Aiko Iwata-Otsubo, Alyssa L Ritter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2022
Expanding the phenotypic spectrum of ARCN1-related syndromeAlyssa L Ritter, Jessica Gold, Hiroshi Hayashi, et al.
Journal of Medical Entomology|November 23, 2019
Infected Mosquitoes Have Altered Behavior to Repellents: A Systematic Review and Meta-analysisMarc J Lajeunesse, Daniel A Avello, Morgan S Behrmann, et al.
Journal of Medical Genetics|March 2, 2022
Consolidation of the clinical and genetic definition of a <i>SOX4-</i>related neurodevelopmental syndromeMarco Angelozzi, Anirudha Karvande, Arnaud N Molin, et al.
Human Mutation|December 3, 2021
The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorderSmitha Kumble, Amanda M Levy, Jaya Punetha, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2020
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variantsLi Xin Zhang, Gabrielle Lemire, Claudia Gonzaga-Jauregui, et al.
Pageof 29

Showing results (281-290 of 287) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 287 results.
Frontiers in Molecular Neuroscience|April 8, 2017
Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD)McKenzie L Ritter, Wei Guo, Jack F Samuels, et al.
American Journal of Human Genetics|October 8, 2019
Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive ImpairmentSarah K Fiordaliso, Aiko Iwata-Otsubo, Alyssa L Ritter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2022
Expanding the phenotypic spectrum of ARCN1-related syndromeAlyssa L Ritter, Jessica Gold, Hiroshi Hayashi, et al.
Journal of Medical Entomology|November 23, 2019
Infected Mosquitoes Have Altered Behavior to Repellents: A Systematic Review and Meta-analysisMarc J Lajeunesse, Daniel A Avello, Morgan S Behrmann, et al.
Journal of Medical Genetics|March 2, 2022
Consolidation of the clinical and genetic definition of a <i>SOX4-</i>related neurodevelopmental syndromeMarco Angelozzi, Anirudha Karvande, Arnaud N Molin, et al.
Human Mutation|December 3, 2021
The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorderSmitha Kumble, Amanda M Levy, Jaya Punetha, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2020
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variantsLi Xin Zhang, Gabrielle Lemire, Claudia Gonzaga-Jauregui, et al.
Pageof 29