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International Journal of Molecular Sciences|March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) SyndromeKyle 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 featuresJennifer 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 defectsDouglas C Bittel, Merlin G Butler, Nataliya Kibiryeva, et al.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.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.Alcoholism, Clinical and Experimental Research|June 17, 2011
The contribution of parental alcohol use disorders and other psychiatric illness to the risk of alcohol use disorders in the offspringHolger J Sørensen, Ann M Manzardo, Joachim Knop, et al.Journal of Studies on Alcohol|December 8, 2005
Neonatal vitamin K might reduce vulnerability to alcohol dependence in Danish menAnn M Manzardo, Elizabeth C Penick, Joachim Knop, 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.Pageof 26