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Current Issues in Molecular Biology
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January 30, 2026
Integrated Genetic and Protein Mechanisms Underlying Glucagon-like Peptide-1 Receptor Agonists in Treating Diabetes Mellitus and Weight Loss
Lucas Francis, Merlin G Butler
The Endocrinologist
|
August 30, 2016
Prader-Willi Syndrome: Clinical and Genetic Findings
Merlin G Butler, Travis Thompson
Journal of Pediatric Genetics
|
May 8, 2019
Classic Ehlers-Danlos Syndrome in a Son and Father with a Heart Transplant Performed in the Father
Paushpala Sen, Merlin G Butler
Journal of Assisted Reproduction and Genetics
|
May 28, 2011
Umbilical cord blood banking: an update
Merlin G Butler, Jay E Menitove
Journal of Pediatric Genetics
|
October 14, 2014
Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome
Adria M Jerkovich, Merlin G Butler
Clinical Genetics
|
September 18, 2024
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A review
Amin J Barakat, Merlin G Butler
Frontiers in Genetics
|
June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databases
Waheeda A Hossain, Merlin G Butler
International Journal of Molecular Sciences
|
May 10, 2020
The 15q11.2 BP1-BP2 Microdeletion (<i>Burnside-Butler</i>) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes
Syed K Rafi, Merlin G Butler
Expert Reviews in Molecular Medicine
|
July 26, 2005
Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology
Douglas C Bittel, Merlin G Butler
International Journal of Molecular Sciences
|
February 18, 2015
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
Devin M Cox, Merlin G Butler
Page
of 26
Search research articles
Search
Showing results (31-40 of 257) with videos related to
Sort By:
Page
of 26
Current Issues in Molecular Biology
|
January 30, 2026
Integrated Genetic and Protein Mechanisms Underlying Glucagon-like Peptide-1 Receptor Agonists in Treating Diabetes Mellitus and Weight Loss
Lucas Francis, Merlin G Butler
The Endocrinologist
|
August 30, 2016
Prader-Willi Syndrome: Clinical and Genetic Findings
Merlin G Butler, Travis Thompson
Journal of Pediatric Genetics
|
May 8, 2019
Classic Ehlers-Danlos Syndrome in a Son and Father with a Heart Transplant Performed in the Father
Paushpala Sen, Merlin G Butler
Journal of Assisted Reproduction and Genetics
|
May 28, 2011
Umbilical cord blood banking: an update
Merlin G Butler, Jay E Menitove
Journal of Pediatric Genetics
|
October 14, 2014
Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome
Adria M Jerkovich, Merlin G Butler
Clinical Genetics
|
September 18, 2024
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A review
Amin J Barakat, Merlin G Butler
Frontiers in Genetics
|
June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databases
Waheeda A Hossain, Merlin G Butler
International Journal of Molecular Sciences
|
May 10, 2020
The 15q11.2 BP1-BP2 Microdeletion (<i>Burnside-Butler</i>) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes
Syed K Rafi, Merlin G Butler
Expert Reviews in Molecular Medicine
|
July 26, 2005
Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology
Douglas C Bittel, Merlin G Butler
International Journal of Molecular Sciences
|
February 18, 2015
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
Devin M Cox, Merlin G Butler
Page
of 26