par Grolaux, Robin 
;Hardy, Alexis ;Olsen, Catharina ;Van Dooren, Sonia;Smits, Guillaume ;Defrance, Matthieu
Référence Clinical Epigenetics, 14, 1
Publication Publié, 2022-12-01
;Hardy, Alexis ;Olsen, Catharina ;Van Dooren, Sonia;Smits, Guillaume ;Defrance, Matthieu Référence Clinical Epigenetics, 14, 1
Publication Publié, 2022-12-01
Article révisé par les pairs
| Titre: |
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| Auteur: | Grolaux, Robin; Hardy, Alexis; Olsen, Catharina; Van Dooren, Sonia; Smits, Guillaume; Defrance, Matthieu |
| Informations sur la publication: | Clinical Epigenetics, 14, 1 |
| Statut de publication: | Publié, 2022-12-01 |
| Sujet CREF: | Biologie cellulaire |
| Biologie générale | |
| Mots-clés: | Beckwith–Wiedemann syndrome |
| Congenital disease | |
| Differentially methylated regions | |
| DNA methylation | |
| Epivariation | |
| Imprinting | |
| Multilocus imprinting disturbance | |
| Neurodevelopmental disorders | |
| Optimization | |
| Rare diseases | |
| Single patient | |
| Statistical method | |
| Note générale: | SCOPUS: ar.j |
| Langue: | Anglais |
| Identificateurs: | urn:issn:1868-7075 |
| info:doi/10.1186/s13148-022-01403-7 | |
| info:pii/1403 | |
| info:scp/85144228481 | |
| info:pmid/36527161 |
