Cargando…
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny
Beckwith–Wiedemann syndrome (BWS, OMIM # 130650) is an imprinting disorder, associated with overgrowth and increased risk of embryonal tumors. Patients carrying hypomethylation in the KCNQ1OT1:TSS DMR (11p15.5) show MLID (Multilocus Imprinting Disturbance) upon epimutations at other imprinted region...
Autores principales: | Tannorella, Pierpaola, Calzari, Luciano, Daolio, Cecilia, Mainini, Ester, Vimercati, Alessandro, Gentilini, Davide, Soli, Fiorenza, Pedrolli, Annalisa, Bonati, Maria Teresa, Larizza, Lidia, Russo, Silvia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941822/ https://www.ncbi.nlm.nih.gov/pubmed/35317853 http://dx.doi.org/10.1186/s13148-022-01262-2 |
Ejemplares similares
-
Beckwith-Wiedemann syndrome
por: Mishra, Deeksha, et al.
Publicado: (2023) -
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
por: Calvello, Mariarosaria, et al.
Publicado: (2013) -
Case report: a typical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum
por: Vimercati, Alessandro, et al.
Publicado: (2023) -
Sonographic Assessment of Renal Growth in Patients with Beckwith-Wiedemann
Syndrome: The Beckwith-Wiedemann Syndrome Renal Nomogram
por: Ortiz-Neira, Clara L, et al.
Publicado: (2009) -
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith–Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
por: Luca, Maria, et al.
Publicado: (2023)