Modeling familial predictors of proband outcomes in neurogenetic disorders: initial application in XYY syndrome

BACKGROUND: Disorders of gene dosage can significantly increase risk for psychopathology, but outcomes vary greatly amongst carriers of any given chromosomal aneuploidy or sub-chromosomal copy number variation (CNV). One potential path to advance precision medicine for neurogenetic disorders is mode...

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Detalles Bibliográficos
Autores principales: Wilson, Kathleen E., Fish, Ari M., Mankiw, Catherine, Xenophontos, Anastasia, Warling, Allysa, Whitman, Ethan, Clasen, Liv, Torres, Erin, Blumenthal, Jonathan, Raznahan, Armin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986517/
https://www.ncbi.nlm.nih.gov/pubmed/33752588
http://dx.doi.org/10.1186/s11689-021-09360-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986517/
https://www.ncbi.nlm.nih.gov/pubmed/33752588
http://dx.doi.org/10.1186/s11689-021-09360-7

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