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Merlin G Butler

Showing results (241-250 of 257) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2013
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technologyJune-Anne Gold, Chelsey Ruth, Kathryn Osann, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2023
Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled TrialJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.
JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Obesity (Silver Spring, Md.)|November 3, 2023
Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: results from long-term open-label studyJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.
The Journal of Clinical Investigation|December 13, 2016
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndromeLisa C Burnett, Charles A LeDuc, Carlos R Sulsona, et al.
Journal of Clinical Medicine|October 13, 2021
Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel DiscussionKarlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, et al.
Pageof 26

Showing results (241-250 of 257) with videos related to

Sort By:
Pageof 26
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2013
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technologyJune-Anne Gold, Chelsey Ruth, Kathryn Osann, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
Human Genetics|March 2, 2011
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayRachel D Burnside, Romela Pasion, Fady M Mikhail, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2023
Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled TrialJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.
JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Obesity (Silver Spring, Md.)|November 3, 2023
Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: results from long-term open-label studyJennifer L Miller, Evelien Gevers, Nicola Bridges, et al.
The Journal of Clinical Investigation|December 13, 2016
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndromeLisa C Burnett, Charles A LeDuc, Carlos R Sulsona, et al.
Journal of Clinical Medicine|October 13, 2021
Hypogonadism in Adult Males with Prader-Willi Syndrome-Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel DiscussionKarlijn Pellikaan, Yassine Ben Brahim, Anna G W Rosenberg, et al.
Pageof 26