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AMA Journal of Ethics
|
October 1, 2025
What Is the Nature and Scope of Physicians' Duties of Care to Patients Without a Diagnosis?
April Hall, Bryn D Webb, M Stephen Meyn
Journal of Translational Genetics and Genomics
|
January 11, 2021
Mitochondrial translation defects and human disease
Bryn D Webb, George A Diaz, Pankaj Prasun
Orphanet Journal of Rare Diseases
|
April 8, 2021
A framework for the evaluation of patients with congenital facial weakness
Bryn D Webb, Irini Manoli, Elizabeth C Engle, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2024
Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia
Lisa M Karger, Bryn D Webb, Lisa Edelmann, et al.
American Journal of Medical Genetics. Part A
|
December 29, 2022
A novel deleterious ETFA promoter variant causative of multiple acyl-CoA dehydrogenase deficiency
Pankaj Prasun, Anthony Evans, Emalyn Cork, et al.
European Journal of Human Genetics : EJHG
|
April 12, 2021
Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis
Bryn D Webb, Hilary Hotchkiss, Pankaj Prasun, et al.
The Application of Clinical Genetics
|
September 14, 2016
Identification of a novel pathogenic OTOF variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population
Anastasia M Fedick, Chaim Jalas, Ananya Swaroop, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
December 10, 2014
Quantitative Assessment of Facial Asymmetry Using Three-Dimensional Surface Imaging in Adults: Validating the Precision and Repeatability of a Global Approach
Davida Kornreich, Adele A Mitchell, Bryn D Webb, et al.
Expert Review of Molecular Diagnostics
|
October 29, 2014
Evaluation of the Affymetrix CytoScan(®) Dx Assay for developmental delay
Bryn D Webb, Rebecca J Scharf, Emily A Spear, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
August 15, 2014
Mirror movements identified in patients with moebius syndrome
Bryn D Webb, Tamiesha Frempong, Thomas P Naidich, et al.
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of 6
Search research articles
Search
Showing results (1-10 of 51) with videos related to
Sort By:
Page
of 6
AMA Journal of Ethics
|
October 1, 2025
What Is the Nature and Scope of Physicians' Duties of Care to Patients Without a Diagnosis?
April Hall, Bryn D Webb, M Stephen Meyn
Journal of Translational Genetics and Genomics
|
January 11, 2021
Mitochondrial translation defects and human disease
Bryn D Webb, George A Diaz, Pankaj Prasun
Orphanet Journal of Rare Diseases
|
April 8, 2021
A framework for the evaluation of patients with congenital facial weakness
Bryn D Webb, Irini Manoli, Elizabeth C Engle, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2024
Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia
Lisa M Karger, Bryn D Webb, Lisa Edelmann, et al.
American Journal of Medical Genetics. Part A
|
December 29, 2022
A novel deleterious ETFA promoter variant causative of multiple acyl-CoA dehydrogenase deficiency
Pankaj Prasun, Anthony Evans, Emalyn Cork, et al.
European Journal of Human Genetics : EJHG
|
April 12, 2021
Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis
Bryn D Webb, Hilary Hotchkiss, Pankaj Prasun, et al.
The Application of Clinical Genetics
|
September 14, 2016
Identification of a novel pathogenic OTOF variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population
Anastasia M Fedick, Chaim Jalas, Ananya Swaroop, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
December 10, 2014
Quantitative Assessment of Facial Asymmetry Using Three-Dimensional Surface Imaging in Adults: Validating the Precision and Repeatability of a Global Approach
Davida Kornreich, Adele A Mitchell, Bryn D Webb, et al.
Expert Review of Molecular Diagnostics
|
October 29, 2014
Evaluation of the Affymetrix CytoScan(®) Dx Assay for developmental delay
Bryn D Webb, Rebecca J Scharf, Emily A Spear, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)
|
August 15, 2014
Mirror movements identified in patients with moebius syndrome
Bryn D Webb, Tamiesha Frempong, Thomas P Naidich, et al.
Page
of 6