Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.

Kim, Hwa Young; Shin, Choong Ho; Shin, Chang Ho; Ko, Jung Min

Kim, Hwa Young; Shin, Choong Ho; Shin, Chang Ho; Ko, Jung Min.

Afiliación

Kim HY; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University Bundang Hospital, Seongnam, Korea.
Shin CH; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University College of Medicine, Seoul, Korea.
Shin CH; Department of Orthopaedics, Division of Pediatric Orthopedics, Seoul National University College of Medicine, Seoul, Korea.
Ko JM; Department of Pediatrics, Division of Clinical Genetics, Seoul National University College of Medicine, Seoul, Korea.

PLoS One ; 18(8): e0290450, 2023.

Article en En | MEDLINE | ID: mdl-37594968

Asunto(s)

Metilación de ADN; Impresión Genómica; Humanos; Exoma; Cromosomas Humanos Par 1; Cromosomas Humanos Par 6

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Impresión Genómica / Metilación de ADN Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google