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Merlin G Butler

Showing results (231-240 of 257) with videos related to

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American Journal of Medical Genetics. Part A|April 6, 2011
Nutritional phases in Prader-Willi syndromeJennifer L Miller, Christy H Lynn, Danielle C Driscoll, et al.
American Journal on Intellectual and Developmental Disabilities|July 10, 2014
Risk factors for self-injury, aggression, and stereotyped behavior among young children at risk for intellectual and developmental disabilitiesStephen R Schroeder, Janet G Marquis, R Matthew Reese, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 23, 2015
Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndromeGabriela L Bravo, Albert B Poje, Iago Perissinotti, et al.
Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.
Journal of Medical Genetics|May 7, 2018
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort studyMerlin G Butler, Samantha N Hartin, Waheeda A Hossain, et al.
Journal of Child and Adolescent Psychopharmacology|March 18, 2015
Loxapine add-on for adolescents and adults with autism spectrum disorders and irritabilityJessica A Hellings, Gregory Reed, Sharon E Cain, et al.
International Journal of Molecular Sciences|May 13, 2023
Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader-Willi SyndromeLawrence P Richer, Qiming Tan, Merlin G Butler, et al.
Archives of Pathology & Laboratory Medicine|July 13, 2006
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for yearsArthur R Brothman, Nancy R Schneider, Irene Saikevych, et al.
Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Pageof 26

Showing results (231-240 of 257) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics. Part A|April 6, 2011
Nutritional phases in Prader-Willi syndromeJennifer L Miller, Christy H Lynn, Danielle C Driscoll, et al.
American Journal on Intellectual and Developmental Disabilities|July 10, 2014
Risk factors for self-injury, aggression, and stereotyped behavior among young children at risk for intellectual and developmental disabilitiesStephen R Schroeder, Janet G Marquis, R Matthew Reese, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 23, 2015
Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndromeGabriela L Bravo, Albert B Poje, Iago Perissinotti, et al.
Translational Psychiatry|October 29, 2020
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disordersEmma K Baker, Merlin G Butler, Samantha N Hartin, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.
Journal of Medical Genetics|May 7, 2018
Molecular genetic classification in Prader-Willi syndrome: a multisite cohort studyMerlin G Butler, Samantha N Hartin, Waheeda A Hossain, et al.
Journal of Child and Adolescent Psychopharmacology|March 18, 2015
Loxapine add-on for adolescents and adults with autism spectrum disorders and irritabilityJessica A Hellings, Gregory Reed, Sharon E Cain, et al.
International Journal of Molecular Sciences|May 13, 2023
Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader-Willi SyndromeLawrence P Richer, Qiming Tan, Merlin G Butler, et al.
Archives of Pathology & Laboratory Medicine|July 13, 2006
Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for yearsArthur R Brothman, Nancy R Schneider, Irene Saikevych, et al.
Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Pageof 26