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Pediatric Blood & Cancer
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June 23, 2018
Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor
Suzanne P MacFarland, Kelly A Duffy, Tricia R Bhatti, et al.
American Journal of Medical Genetics. Part A
|
May 9, 2019
Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome
Jennifer L Cohen, Kelly A Duffy, Brian J Sajorda, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2026
High-Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient-Reported Data
Andrew M George, Bamelak T Duki, Zoe S Katz, et al.
Nature Reviews. Disease Primers
|
June 29, 2023
Imprinting disorders
Thomas Eggermann, David Monk, Guiomar Perez de Nanclares, et al.
Frontiers in Pediatrics
|
August 2, 2021
Case Report: Two Distinct Focal Congenital Hyperinsulinism Lesions Resulting From Separate Genetic Events
Elizabeth Rosenfeld, Lauren Mitteer, Kara Boodhansingh, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2025
Growth Charts for Children With Beckwith-Wiedemann Spectrum
Saskia M Maas, Peter Lauffer, Guido Cocchi, et al.
Communications Biology
|
March 26, 2025
Single-nucleus multiomic analysis of Beckwith-Wiedemann syndrome liver reveals PPARA signaling enrichment and metabolic dysfunction
Snehal Nirgude, Elisia D Tichy, Zhengfeng Liu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 31, 2019
Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management
Kelly A Duffy, Christopher M Cielo, Jennifer L Cohen, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2024
Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review
Alex F Nisbet, Aravind Viswanathan, Andrew M George, et al.
Journal of Medical Genetics
|
November 8, 2015
Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome
Jennifer M Kalish, Kara E Boodhansingh, Tricia R Bhatti, et al.
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of 12
Search research articles
Search
Showing results (81-90 of 112) with videos related to
Sort By:
Page
of 12
Pediatric Blood & Cancer
|
June 23, 2018
Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor
Suzanne P MacFarland, Kelly A Duffy, Tricia R Bhatti, et al.
American Journal of Medical Genetics. Part A
|
May 9, 2019
Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome
Jennifer L Cohen, Kelly A Duffy, Brian J Sajorda, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2026
High-Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient-Reported Data
Andrew M George, Bamelak T Duki, Zoe S Katz, et al.
Nature Reviews. Disease Primers
|
June 29, 2023
Imprinting disorders
Thomas Eggermann, David Monk, Guiomar Perez de Nanclares, et al.
Frontiers in Pediatrics
|
August 2, 2021
Case Report: Two Distinct Focal Congenital Hyperinsulinism Lesions Resulting From Separate Genetic Events
Elizabeth Rosenfeld, Lauren Mitteer, Kara Boodhansingh, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2025
Growth Charts for Children With Beckwith-Wiedemann Spectrum
Saskia M Maas, Peter Lauffer, Guido Cocchi, et al.
Communications Biology
|
March 26, 2025
Single-nucleus multiomic analysis of Beckwith-Wiedemann syndrome liver reveals PPARA signaling enrichment and metabolic dysfunction
Snehal Nirgude, Elisia D Tichy, Zhengfeng Liu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 31, 2019
Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management
Kelly A Duffy, Christopher M Cielo, Jennifer L Cohen, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2024
Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review
Alex F Nisbet, Aravind Viswanathan, Andrew M George, et al.
Journal of Medical Genetics
|
November 8, 2015
Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome
Jennifer M Kalish, Kara E Boodhansingh, Tricia R Bhatti, et al.
Page
of 12