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Pediatrics|March 3, 2004
Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomyMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.Journal of Neurochemistry|November 1, 2006
Biphasic alterations in serotonin-1B (5-HT1B) receptor function during abstinence from extended cocaine self-administrationLaura E O'Dell, Ann M Manzardo, Ilham Polis, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndromeSigan L Hartley, William E Maclean, Merlin G Butler, et al.American Journal of Medical Genetics. Part A|December 28, 2020
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disordersJacob Steinle, Waheeda A Hossain, Scott Lovell, et al.American Journal of Medical Genetics. Part A|January 19, 2010
An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotypeMerlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.Cancer Genetics and Cytogenetics|November 1, 2006
Clonality studies in sacral chordomaLance Klingler, Rita Trammell, D Gordon Allan, et al.American Journal of Medical Genetics. Part A|May 16, 2003
Coenzyme Q10 levels in Prader-Willi syndrome: comparison with obese and non-obese subjectsMerlin G Butler, Majed Dasouki, Doug Bittel, et al.Genomics|December 21, 2004
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPDDouglas C Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2022
Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader-Willi syndromeMoris A Angulo, Merlin G Butler, Waheeda A Hossain, et al.American Journal of Medical Genetics. Part A|February 14, 2006
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysisDouglas C Bittel, Nataliya Kibiryeva, Majed Dasouki, et al.Pageof 26