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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.
Gene|November 6, 2013
Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic servicesJennifer L Roberts, Karine Hovanes, Majed Dasouki, 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.
Drug and Alcohol Dependence|April 25, 2015
Change in psychiatric symptomatology after benfotiamine treatment in males is related to lifetime alcoholism severityAnn M Manzardo, Tiffany Pendleton, Albert Poje, et al.
Genes|July 24, 2019
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire SurveyAnn M Manzardo, Janalee Heinemann, Barbara McManus, 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.
Progress in Pediatric Cardiology|May 23, 2017
Gene expression in pediatric heart disease with emphasis on conotruncal defectsDouglas C Bittel, Nataliya Kibiryeva, James E O'Brien, et al.
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