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Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting

Most major neuropsychiatric outcomes of concern to families are not detectable by prenatal ultrasound. The introduction of genome-wide chromosomal microarray analysis to prenatal clinical diagnostic testing has increased the detection of pathogenic 22q11.2 deletions, which cause the most common geno...

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Publicado en:Prenat Diagn
Autores principales: Bassett, Anne S., Costain, Gregory, Marshall, Christian R.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5243851/
https://ncbi.nlm.nih.gov/pubmed/27718271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.4935
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