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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 18, 2006
C-reactive protein levels in subjects with Prader-Willi syndrome and obesity
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
International Journal of Molecular Sciences
|
February 25, 2015
Pharmacogenetics informed decision making in adolescent psychiatric treatment: a clinical case report
Teri Smith, Susan Sharp, Ann M Manzardo, et al.
The Journal of Rare Disorders
|
January 15, 2019
STARTLE RESPONSE ANALYSIS OF FOOD-IMAGE PROCESSING IN PRADER-WILLI SYNDROME
Alex Gabrielli, Albert B Poje, Ann Manzardo, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
March 23, 2011
TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome
Elisabeth M Dykens, Elizabeth Roof, Douglas Bittel, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
December 24, 2017
Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome
Merlin G Butler, Waheeda Hossain, Maaz Hassan, et al.
International Journal of Molecular Medicine
|
March 9, 2005
Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome
Zohreh Talebizadeh, Nataliya Kibiryeva, Douglas C Bittel, et al.
Alcoholism, Clinical and Experimental Research
|
June 4, 2014
Exon microarray analysis of human dorsolateral prefrontal cortex in alcoholism
Ann M Manzardo, Sumedha Gunewardena, Kun Wang, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review
Samantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2009
Morning melatonin levels in Prader-Willi syndrome
Merlin G Butler, Duane T Brandau, Mariana F Theodoro, et al.
BMC Medical Genomics
|
August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study
Olivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
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of 26
Search research articles
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Showing results (111-120 of 257) with videos related to
Sort By:
Page
of 26
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 18, 2006
C-reactive protein levels in subjects with Prader-Willi syndrome and obesity
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, et al.
International Journal of Molecular Sciences
|
February 25, 2015
Pharmacogenetics informed decision making in adolescent psychiatric treatment: a clinical case report
Teri Smith, Susan Sharp, Ann M Manzardo, et al.
The Journal of Rare Disorders
|
January 15, 2019
STARTLE RESPONSE ANALYSIS OF FOOD-IMAGE PROCESSING IN PRADER-WILLI SYNDROME
Alex Gabrielli, Albert B Poje, Ann Manzardo, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
March 23, 2011
TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome
Elisabeth M Dykens, Elizabeth Roof, Douglas Bittel, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
December 24, 2017
Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome
Merlin G Butler, Waheeda Hossain, Maaz Hassan, et al.
International Journal of Molecular Medicine
|
March 9, 2005
Ghrelin, peptide YY and their receptors: gene expression in brain from subjects with and without Prader-Willi syndrome
Zohreh Talebizadeh, Nataliya Kibiryeva, Douglas C Bittel, et al.
Alcoholism, Clinical and Experimental Research
|
June 4, 2014
Exon microarray analysis of human dorsolateral prefrontal cortex in alcoholism
Ann M Manzardo, Sumedha Gunewardena, Kun Wang, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review
Samantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
American Journal of Medical Genetics. Part A
|
July 17, 2009
Morning melatonin levels in Prader-Willi syndrome
Merlin G Butler, Duane T Brandau, Mariana F Theodoro, et al.
BMC Medical Genomics
|
August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study
Olivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
Page
of 26