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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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| 出版年: | Prenat Diagn |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2016
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| 主題: | |
| オンライン･アクセス: | 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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