Results 171 to 180 of about 14,149 (242)

Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome

open access: yesDevelopment, 2017
Vir B. Singh   +6 more
semanticscholar   +1 more source

Type 1 Diabetes in a Pediatric Patient With Beckwith-Wiedemann Syndrome. [PDF]

open access: yesJCEM Case Rep
Ehsan L   +4 more
europepmc   +1 more source

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome

open access: yesEuropean Journal of Human Genetics, 2015
A. Mussa   +20 more
semanticscholar   +1 more source

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.

open access: yesHuman Molecular Genetics, 2002
R. Weksberg   +15 more
semanticscholar   +1 more source

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

open access: yesEuropean Journal of Human Genetics, 2005
W. Cooper   +13 more
semanticscholar   +1 more source

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome. [PDF]

open access: yesPlast Reconstr Surg Glob Open
Binhezaim A   +3 more
europepmc   +1 more source

Single-nucleus multiomic analysis of Beckwith-Wiedemann syndrome liver reveals PPARA signaling enrichment and metabolic dysfunction. [PDF]

open access: yesCommun Biol
Nirgude S   +13 more
europepmc   +1 more source

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