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Integration Of Microarray Technology Into Prenatal Diagnosis: Counseling Issues Generated During The NICHD Clinical Trial

Cytogenetic microarray analysis (CMA) in prenatal testing detects chromosome abnormalities and new genetic syndromes that would be missed by conventional cytogenetics and has the potential to significantly enhance prenatal genetic evaluation. A large NICHD-sponsored multi-centered trial to assess th...

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Detalhes bibliográficos
Publicado no:Prenat Diagn
Main Authors: Wapner, Ronald J., Driscoll, Deborah A., Simpson, Joe Leigh
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4251739/
https://ncbi.nlm.nih.gov/pubmed/22467170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.3863
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