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Journal of Pediatric Genetics
|
September 13, 2016
A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome
Devin M Cox, Merlin G Butler
Medical Anthropology Quarterly
|
October 4, 2016
Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning
F John Meaney, Merlin G Butler
Genes
|
February 26, 2025
Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric Associations
Ann C Genovese, Merlin G Butler
American Journal of Medical Genetics. Part A
|
October 3, 2022
Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings
Merlin G Butler, Neil Cowen, Anish Bhatnagar
Frontiers in Genetics
|
December 17, 2020
Pharmacodynamic Gene Testing in Prader-Willi Syndrome
Janice Forster, Jessica Duis, Merlin G Butler
International Journal of Molecular Sciences
|
October 14, 2022
Genetics of Obesity in Humans: A Clinical Review
Ranim Mahmoud, Virginia Kimonis, Merlin G Butler
Genes
|
September 27, 2025
RNA Polymerase I Dysfunction Underlying Craniofacial Syndromes: Integrated Genetic Analysis Reveals Parallels to 22q11.2 Deletion Syndrome
Spencer Silvey, Scott Lovell, Merlin G Butler
International Journal of Molecular Sciences
|
February 11, 2023
Clinical Trials in Prader-Willi Syndrome: A Review
Ranim Mahmoud, Virginia Kimonis, Merlin G Butler
Genes
|
January 27, 2021
Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi Syndrome
Janice Forster, Jessica Duis, Merlin G Butler
American Journal of Medical Genetics. Part A
|
March 3, 2004
Eye abnormalities in Fryns syndrome
Diane M Pierson, Eugenio Taboada, Merlin G Butler
Page
of 26
Search research articles
Search
Showing results (51-60 of 257) with videos related to
Sort By:
Page
of 26
Journal of Pediatric Genetics
|
September 13, 2016
A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome
Devin M Cox, Merlin G Butler
Medical Anthropology Quarterly
|
October 4, 2016
Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning
F John Meaney, Merlin G Butler
Genes
|
February 26, 2025
Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric Associations
Ann C Genovese, Merlin G Butler
American Journal of Medical Genetics. Part A
|
October 3, 2022
Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings
Merlin G Butler, Neil Cowen, Anish Bhatnagar
Frontiers in Genetics
|
December 17, 2020
Pharmacodynamic Gene Testing in Prader-Willi Syndrome
Janice Forster, Jessica Duis, Merlin G Butler
International Journal of Molecular Sciences
|
October 14, 2022
Genetics of Obesity in Humans: A Clinical Review
Ranim Mahmoud, Virginia Kimonis, Merlin G Butler
Genes
|
September 27, 2025
RNA Polymerase I Dysfunction Underlying Craniofacial Syndromes: Integrated Genetic Analysis Reveals Parallels to 22q11.2 Deletion Syndrome
Spencer Silvey, Scott Lovell, Merlin G Butler
International Journal of Molecular Sciences
|
February 11, 2023
Clinical Trials in Prader-Willi Syndrome: A Review
Ranim Mahmoud, Virginia Kimonis, Merlin G Butler
Genes
|
January 27, 2021
Pharmacogenetic Testing of Cytochrome P450 Drug Metabolizing Enzymes in a Case Series of Patients with Prader-Willi Syndrome
Janice Forster, Jessica Duis, Merlin G Butler
American Journal of Medical Genetics. Part A
|
March 3, 2004
Eye abnormalities in Fryns syndrome
Diane M Pierson, Eugenio Taboada, Merlin G Butler
Page
of 26