Chromosomal microarray analysis in the investigation of prenatally diagnosed congenital heart disease.

Mustafa, Hiba J; Jacobs, Katherine M; Tessier, Katelyn M; Narasimhan, Shanti L; Tofte, Alena N; McCarter, Allison R; Cross, Sarah N

Mustafa, Hiba J; Jacobs, Katherine M; Tessier, Katelyn M; Narasimhan, Shanti L; Tofte, Alena N; McCarter, Allison R; Cross, Sarah N.

Afiliación

Mustafa HJ; Department of Obstetrics, Gynecology & Women's Health, University of Minnesota, Eden Prairie, MN.
Jacobs KM; Department of Obstetrics, Gynecology & Women's Health, University of Minnesota, Eden Prairie, MN.
Tessier KM; Biostatistics Core, Masonic Cancer Center, University of Minnesota, Eden Prairie, MN.
Narasimhan SL; Department of Pediatric Cardiology, University of Minnesota, Eden Prairie, MN.
Tofte AN; Department of Obstetrics, Gynecology & Women's Health, University of Minnesota, Eden Prairie, MN.
McCarter AR; Department of Obstetrics, Gynecology & Women's Health, University of Minnesota, Eden Prairie, MN.
Cross SN; Department of Obstetrics, Gynecology & Women's Health, University of Minnesota, Eden Prairie, MN.

Am J Obstet Gynecol MFM ; 2(1): 100078, 2020 02.

Article en En | MEDLINE | ID: mdl-33345990

Asunto(s)

Cardiopatías Congénitas; Transposición de los Grandes Vasos; Femenino; Cardiopatías Congénitas/diagnóstico; Humanos; Cariotipificación; Análisis por Micromatrices; Embarazo; Estudios Retrospectivos

Palabras clave

chromosomal abnormalities; congenital heart disease; copy number variants; microarray

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transposición de los Grandes Vasos / Cardiopatías Congénitas Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Am J Obstet Gynecol MFM Año: 2020 Tipo del documento: Article País de afiliación: Mongolia

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