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American Journal of Medical Genetics. Part A|May 23, 2013
Growth hormone receptor (GHR) gene polymorphism and Prader-Willi syndromeMerlin G Butler, Jennifer Roberts, Jena Hayes, et al.
American Journal of Medical Genetics|January 25, 2002
Oculoauriculofrontonasal syndrome (OAFNS) in a nine-month-old maleHolly A Ishmael, Michael L Begleiter, Elizabeth J Regier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2016
Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality surveyMerlin G Butler, Ann M Manzardo, Janalee Heinemann, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Increased plasma chemokine levels in children with Prader-Willi syndromeMerlin G Butler, Waheeda Hossain, Carlos Sulsona, 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.
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