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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.
Journal of Pediatric Psychology|October 31, 2015
A Direct Comparison of Self-Injurious and Stereotyped Motor Behavior Between Preschool-Aged Children With and Without Developmental DelaysJohn Hoch, Lisa Spofford, Adele Dimian, 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.
Plos One|November 18, 2022
Academic Tracker: Software for tracking and reporting publications associated with authors and grantsP Travis Thompson, Christian D Powell, Hunter N B Moseley
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.
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