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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 Disorder
Olivia 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 TRANSMISSION
Stephen 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 cohort
Merlin 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 study
Jennifer 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 Adults
Paula 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 Action
Deepan 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) Syndrome
Kyle 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 features
Jennifer 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 defects
Douglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.
Pediatrics
|
December 10, 2014
Growth charts for non-growth hormone treated Prader-Willi syndrome
Merlin G Butler, Jaehoon Lee, Ann M Manzardo, et al.
Page
of 26
Search research articles
Search
Showing results (191-200 of 257) with videos related to
Sort By:
Page
of 26
International Journal of Molecular Sciences
|
December 2, 2020
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
Olivia 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 TRANSMISSION
Stephen 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 cohort
Merlin 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 study
Jennifer 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 Adults
Paula 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 Action
Deepan 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) Syndrome
Kyle 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 features
Jennifer 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 defects
Douglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.
Pediatrics
|
December 10, 2014
Growth charts for non-growth hormone treated Prader-Willi syndrome
Merlin G Butler, Jaehoon Lee, Ann M Manzardo, et al.
Page
of 26