Chromosomal Microarray Study in Prader-Willi Syndrome

A high-resolution chromosome microarray analysis was performed on 154 consecutive individuals enrolled in the DESTINY PWS clinical trial for Prader-Willi syndrome (PWS). Of these 154 PWS individuals, 87 (56.5%) showed the typical 15q11-q13 deletion subtypes, 62 (40.3%) showed non-deletion maternal d...

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Detalles Bibliográficos
Autores principales: Butler, Merlin G., Hossain, Waheeda A., Cowen, Neil, Bhatnagar, Anish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863005/
https://www.ncbi.nlm.nih.gov/pubmed/36674736
http://dx.doi.org/10.3390/ijms24021220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863005/
https://www.ncbi.nlm.nih.gov/pubmed/36674736
http://dx.doi.org/10.3390/ijms24021220

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