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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Pediatr
Prif Awduron: Butler, Merlin G., Duis, Jessica
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7235373/
https://ncbi.nlm.nih.gov/pubmed/32478012
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2020.00154
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