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Merlin G Butler

Showing results (191-200 of 257) with videos related to

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International Journal of Molecular Sciences|December 2, 2020
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum DisorderOlivia J Veatch, Merlin G Butler, Sarah H Elsea, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|February 7, 2017
FAMILIAL LARYNGEAL WEB IN THREE GENERATIONS WITH PROBABLE AUTOSOMAL DOMINANT TRANSMISSIONStephen M Strakowski, Merlin G Butler, James W Cheek, et al.
American Journal of Medical Genetics. Part A|June 22, 2019
Birth seasonality studies in a large Prader-Willi syndrome cohortMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Oxytocin treatment in children with Prader-Willi syndrome: A double-blind, placebo-controlled, crossover studyJennifer L Miller, Roy Tamura, Merlin G Butler, et al.
Journal of Child Sexual Abuse|June 19, 2025
Sex-Dependent Effects of <i>MAOA</i> Genotypes on the Relations Between Childhood Sexual Abuse, Aggression, and Cannabis Use in Emerging AdultsPaula J Fite, Annie L Ryder, Selena Baca, et al.
International Journal of Molecular Sciences|July 29, 2023
The Arduous Path to Drug Approval for the Management of Prader-Willi Syndrome: A Historical Perspective and Call to ActionDeepan Singh, Jennifer L Miller, Edward Robert Wassman, et al.
International Journal of Molecular Sciences|March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) SyndromeKyle W Davis, Moises Serrano, Sara Loddo, et al.
Case Reports in Genetics|July 4, 2014
Clinical report of a 17q12 microdeletion with additionally unreported clinical featuresJennifer L Roberts, Stephanie K Gandomi, Melissa Parra, et al.
BMC Medical Genomics|January 7, 2011
Gene expression in cardiac tissues from infants with idiopathic conotruncal defectsDouglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.
Pediatrics|December 10, 2014
Growth charts for non-growth hormone treated Prader-Willi syndromeMerlin G Butler, Jaehoon Lee, Ann M Manzardo, et al.
Pageof 26

Showing results (191-200 of 257) with videos related to

Sort By:
Pageof 26
International Journal of Molecular Sciences|December 2, 2020
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum DisorderOlivia J Veatch, Merlin G Butler, Sarah H Elsea, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|February 7, 2017
FAMILIAL LARYNGEAL WEB IN THREE GENERATIONS WITH PROBABLE AUTOSOMAL DOMINANT TRANSMISSIONStephen M Strakowski, Merlin G Butler, James W Cheek, et al.
American Journal of Medical Genetics. Part A|June 22, 2019
Birth seasonality studies in a large Prader-Willi syndrome cohortMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Oxytocin treatment in children with Prader-Willi syndrome: A double-blind, placebo-controlled, crossover studyJennifer L Miller, Roy Tamura, Merlin G Butler, et al.
Journal of Child Sexual Abuse|June 19, 2025
Sex-Dependent Effects of <i>MAOA</i> Genotypes on the Relations Between Childhood Sexual Abuse, Aggression, and Cannabis Use in Emerging AdultsPaula J Fite, Annie L Ryder, Selena Baca, et al.
International Journal of Molecular Sciences|July 29, 2023
The Arduous Path to Drug Approval for the Management of Prader-Willi Syndrome: A Historical Perspective and Call to ActionDeepan Singh, Jennifer L Miller, Edward Robert Wassman, et al.
International Journal of Molecular Sciences|March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) SyndromeKyle W Davis, Moises Serrano, Sara Loddo, et al.
Case Reports in Genetics|July 4, 2014
Clinical report of a 17q12 microdeletion with additionally unreported clinical featuresJennifer L Roberts, Stephanie K Gandomi, Melissa Parra, et al.
BMC Medical Genomics|January 7, 2011
Gene expression in cardiac tissues from infants with idiopathic conotruncal defectsDouglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.
Pediatrics|December 10, 2014
Growth charts for non-growth hormone treated Prader-Willi syndromeMerlin G Butler, Jaehoon Lee, Ann M Manzardo, et al.
Pageof 26