Chromosome 15 Imprinting Disorders: Genetic Laboratory Methodology and Approaches

Chromosome 15 imprinting disorders include Prader-Willi (PWS) and Angelman (AS) syndromes, which are caused by absent expression from the paternal and maternal alleles in the chromosome 15q11. 2–q13 region, respectively. In addition, chromosome 15q duplication caused by the presence of at least one...

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Detalles Bibliográficos
Autores principales: Butler, Merlin G., Duis, Jessica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235373/
https://www.ncbi.nlm.nih.gov/pubmed/32478012
http://dx.doi.org/10.3389/fped.2020.00154

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235373/
https://www.ncbi.nlm.nih.gov/pubmed/32478012
http://dx.doi.org/10.3389/fped.2020.00154

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