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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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| Pubblicato in: | Prenat Diagn |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2016
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| Soggetti: | |
| Accesso online: | 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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