Methylation-Specific Multiplex Ligation-Dependent Probe Amplification and Identification of Deletion Genetic Subtypes in Prader-Willi Syndrome

Purpose: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are complex neurodevelopmental disorders caused by loss of expression of imprinted genes from the 15q11-q13 region depending on the parent of origin. Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) kits f...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Henkhaus, Rebecca S., Kim, Soo-Jeong, Kimonis, Virginia E., Gold, June-Anne, Dykens, Elisabeth M., Driscoll, Daniel J., Butler, Merlin G.
Format: Artigo
Idioma:Inglês
Publicat: Mary Ann Liebert, Inc. 2012
Matèries:
Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3306590/
https://ncbi.nlm.nih.gov/pubmed/21977908
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2011.0115
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars