Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

OBJECTIVE: To prospectively study the addition of array comparative genomic hybridization (CGH) to the prenatal evaluation of fetal structural anomalies. METHODS: Pregnant women carrying fetuses with a major structural abnormality were recruited at the time of invasive procedure for chromosome analy...

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Publicat a:Prenat Diagn
Autors principals: Kleeman, Linda, Bianchi, Diana W., Shaffer, Lisa G., Rorem, Emily, Cowan, Janet, Craigo, Sabrina D., Tighiouart, Hocine, Wilkins-Haug, Louise E.
Format: Artigo
Idioma:Inglês
Publicat: 2009
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4459708/
https://ncbi.nlm.nih.gov/pubmed/19862770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.2367
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