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Merlin G Butler

Showing results (181-190 of 257) with videos related to

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American Journal of Medical Genetics. Part A|December 25, 2009
An 18-year follow-up report on an infant with a duplication of 9q34Erin L Youngs, Timothy McCord, Jessica A Hellings, et al.
Gene|December 28, 2007
snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctionsPeter S Bazeley, Valery Shepelev, Zohreh Talebizadeh, et al.
Clinical Endocrinology|March 5, 2015
Metabolic profiling in Prader-Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormoneKrystal A Irizarry, James Bain, Merlin G Butler, et al.
Journal of Aggression, Maltreatment & Trauma|December 7, 2020
Relationship Between Body Habitus and Aggression Subtypes Among Healthy Young Adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.
Journal of Autism and Developmental Disorders|February 1, 2005
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?Zohreh Talebizadeh, Douglas C Bittel, Olivia J Veatch, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Steven G McNulty, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
X-chromosome inactivation patterns in females with Prader-Willi syndromeMerlin G Butler, Mariana F Theodoro, Douglas C Bittel, et al.
American Journal of Medical Genetics. Part A|December 18, 2018
Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomesRanim Mahmoud, Preeti Singh, Lan Weiss, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history studyMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.
Cytogenetic and Genome Research|November 29, 2016
Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3)Vy Dang, Abhilasha Surampalli, Ann M Manzardo, et al.
Pageof 26

Showing results (181-190 of 257) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics. Part A|December 25, 2009
An 18-year follow-up report on an infant with a duplication of 9q34Erin L Youngs, Timothy McCord, Jessica A Hellings, et al.
Gene|December 28, 2007
snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctionsPeter S Bazeley, Valery Shepelev, Zohreh Talebizadeh, et al.
Clinical Endocrinology|March 5, 2015
Metabolic profiling in Prader-Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormoneKrystal A Irizarry, James Bain, Merlin G Butler, et al.
Journal of Aggression, Maltreatment & Trauma|December 7, 2020
Relationship Between Body Habitus and Aggression Subtypes Among Healthy Young Adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.
Journal of Autism and Developmental Disorders|February 1, 2005
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?Zohreh Talebizadeh, Douglas C Bittel, Olivia J Veatch, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Steven G McNulty, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
X-chromosome inactivation patterns in females with Prader-Willi syndromeMerlin G Butler, Mariana F Theodoro, Douglas C Bittel, et al.
American Journal of Medical Genetics. Part A|December 18, 2018
Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomesRanim Mahmoud, Preeti Singh, Lan Weiss, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history studyMerlin G Butler, Virginia Kimonis, Elisabeth Dykens, et al.
Cytogenetic and Genome Research|November 29, 2016
Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3)Vy Dang, Abhilasha Surampalli, Ann M Manzardo, et al.
Pageof 26