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Clinical Dysmorphology
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February 26, 2015
A clinical case report and literature review of the 3q29 microdeletion syndrome
Devin M Cox, Merlin G Butler
Cytogenetic and Genome Research
|
April 15, 2015
Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities
Devin M Cox, Merlin G Butler
American Journal of Medical Genetics. Part A
|
August 21, 2012
Development and implementation of electronic growth charts for infants with Prader-Willi syndrome
S Trent Rosenbloom, Merlin G Butler
Genes
|
September 28, 2021
Special Issue: Genetics of Prader-Willi Syndrome
David E Godler, Merlin G Butler
Journal of Assisted Reproduction and Genetics
|
May 1, 2015
Androgen receptor (AR) gene CAG trinucleotide repeat length associated with body composition measures in non-syndromic obese, non-obese and Prader-Willi syndrome individuals
Merlin G Butler, Ann M Manzardo
American Journal of Medical Genetics. Part A
|
February 17, 2007
Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome
Merlin G Butler, Douglas C Bittel
Prader-Willi Perspectives : a Journal of Prader-Willi Syndrome Information for Parents & Professionals
|
September 11, 2018
Atypical Clinical Findings in Prader-Willi Syndrome Patients: Analysis of Survey Data
Merlin G Butler, Peter K Rogan
Genes
|
September 27, 2025
<i>PTEN</i> Gene and Autism: Genetic Underpinnings and Neurodevelopmental Impacts
Ann C Genovese, Merlin G Butler
Brain Sciences
|
April 27, 2024
Behavioral and Psychiatric Disorders in Syndromic Autism
Ann C Genovese, Merlin G Butler
World Journal of Medical Genetics
|
March 28, 2017
Mutation in <i>TNXB</i> gene causes moderate to severe Ehlers-Danlos syndrome
Carolyn S Kaufman, Merlin G Butler
Page
of 26
Search research articles
Search
Showing results (41-50 of 257) with videos related to
Sort By:
Page
of 26
Clinical Dysmorphology
|
February 26, 2015
A clinical case report and literature review of the 3q29 microdeletion syndrome
Devin M Cox, Merlin G Butler
Cytogenetic and Genome Research
|
April 15, 2015
Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities
Devin M Cox, Merlin G Butler
American Journal of Medical Genetics. Part A
|
August 21, 2012
Development and implementation of electronic growth charts for infants with Prader-Willi syndrome
S Trent Rosenbloom, Merlin G Butler
Genes
|
September 28, 2021
Special Issue: Genetics of Prader-Willi Syndrome
David E Godler, Merlin G Butler
Journal of Assisted Reproduction and Genetics
|
May 1, 2015
Androgen receptor (AR) gene CAG trinucleotide repeat length associated with body composition measures in non-syndromic obese, non-obese and Prader-Willi syndrome individuals
Merlin G Butler, Ann M Manzardo
American Journal of Medical Genetics. Part A
|
February 17, 2007
Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome
Merlin G Butler, Douglas C Bittel
Prader-Willi Perspectives : a Journal of Prader-Willi Syndrome Information for Parents & Professionals
|
September 11, 2018
Atypical Clinical Findings in Prader-Willi Syndrome Patients: Analysis of Survey Data
Merlin G Butler, Peter K Rogan
Genes
|
September 27, 2025
<i>PTEN</i> Gene and Autism: Genetic Underpinnings and Neurodevelopmental Impacts
Ann C Genovese, Merlin G Butler
Brain Sciences
|
April 27, 2024
Behavioral and Psychiatric Disorders in Syndromic Autism
Ann C Genovese, Merlin G Butler
World Journal of Medical Genetics
|
March 28, 2017
Mutation in <i>TNXB</i> gene causes moderate to severe Ehlers-Danlos syndrome
Carolyn S Kaufman, Merlin G Butler
Page
of 26