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American Journal of Medical Genetics. Part A|February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and reviewSamantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
BMC Medical Genomics|August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional studyOlivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Preliminary observations of mitochondrial dysfunction in Prader-Willi syndromeMerlin G Butler, Waheeda A Hossain, Robert Tessman, et al.
European Journal of Medical Genetics|September 22, 2011
IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic featuresErin L Youngs, Rebecca Henkhaus, Jessica A Hellings, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|February 11, 2017
TOWNES-BROCKS SYNDROME: REPORT OF THREE ADDITIONAL PATIENTS WITH PREVIOUSLY UNDESCRIBED RENAL AND CARDIAC ABNORMALITIESAmin Y Barakat, Merlin G Butler, James E Salter, et al.
Autism Research and Treatment|August 31, 2012
Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatryMerlin G Butler, Erin L Youngs, Jennifer L Roberts, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|October 4, 2016
NORMATIVE STANDARDS AND COMPARISON OF ANTHROPOMETRIC DATA OF WHITE AND BLACK NEWBORN INFANTSJon M Brandt, G Andrew Allen, Judy L Haynes, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjectsMerlin G Butler, Mariana F Theodoro, Douglas C Bittel, et al.
Dysmorphology and Clinical Genetics : Official Publication of the Center for Birth Defects Information Services, Inc|August 30, 2016
RESTING METABOLIC RATE IN PRADER-WILLI SYNDROMEJames O Hill, Mary Kaler, Bennett Spetalnick, 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.
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