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Merlin G Butler

Showing results (201-210 of 257) with videos related to

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International Journal of Molecular Sciences|February 10, 2021
Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five FamiliesIsaac Baldwin, Robin L Shafer, Waheeda A Hossain, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|February 21, 2018
A descriptive study on selected growth parameters and growth hormone receptor gene in healthy young adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.
International Journal of Molecular Sciences|August 26, 2022
Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and ReviewMerlin G Butler, Waheeda A Hossain, Jacob Steinle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 14, 2012
The neuroanatomy of genetic subtype differences in Prader-Willi syndromeRobyn A Honea, Laura M Holsen, Rebecca J Lepping, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataractsKaren W Gripp, Caitlyn Johnson, Charles I Scott, et al.
American Journal of Medical Genetics. Part A|December 21, 2018
Contributing factors of mortality in Prader-Willi syndromeJennifer Proffitt, Kathryn Osann, Barbara McManus, et al.
Advances in Genomics and Genetics|February 24, 2015
Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromesMerlin G Butler, Kun Wang, Jan D Marshall, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 2, 2007
Gastric rupture and necrosis in Prader-Willi syndromeDavid A Stevenson, Janalee Heinemann, Moris Angulo, et al.
Genetic Testing and Molecular Biomarkers|October 8, 2011
Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndromeRebecca S Henkhaus, Soo-Jeong Kim, Virginia E Kimonis, et al.
Obesity Surgery|August 30, 2011
Letter to the editor: Long-term experience with duodenal switch in adolescentsAnn O Scheimann, Merlin G Butler, Jennifer L Miller, et al.
Pageof 26

Showing results (201-210 of 257) with videos related to

Sort By:
Pageof 26
International Journal of Molecular Sciences|February 10, 2021
Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five FamiliesIsaac Baldwin, Robin L Shafer, Waheeda A Hossain, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|February 21, 2018
A descriptive study on selected growth parameters and growth hormone receptor gene in healthy young adults from the American MidwestSamantha N Hartin, Waheeda A Hossain, Ann M Manzardo, et al.
International Journal of Molecular Sciences|August 26, 2022
Connective Tissue Disorders and Fragile X Molecular Status in Females: A Case Series and ReviewMerlin G Butler, Waheeda A Hossain, Jacob Steinle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 14, 2012
The neuroanatomy of genetic subtype differences in Prader-Willi syndromeRobyn A Honea, Laura M Holsen, Rebecca J Lepping, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataractsKaren W Gripp, Caitlyn Johnson, Charles I Scott, et al.
American Journal of Medical Genetics. Part A|December 21, 2018
Contributing factors of mortality in Prader-Willi syndromeJennifer Proffitt, Kathryn Osann, Barbara McManus, et al.
Advances in Genomics and Genetics|February 24, 2015
Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromesMerlin G Butler, Kun Wang, Jan D Marshall, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 2, 2007
Gastric rupture and necrosis in Prader-Willi syndromeDavid A Stevenson, Janalee Heinemann, Moris Angulo, et al.
Genetic Testing and Molecular Biomarkers|October 8, 2011
Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndromeRebecca S Henkhaus, Soo-Jeong Kim, Virginia E Kimonis, et al.
Obesity Surgery|August 30, 2011
Letter to the editor: Long-term experience with duodenal switch in adolescentsAnn O Scheimann, Merlin G Butler, Jennifer L Miller, et al.
Pageof 26