Prenatal diagnosis of a 7q21.13q22.1 deletion detected using high-resolution microarray

We report a case of de novo 7q interstitial deletion detected by conventional karyotyping and by microarray of amniotic fluid sampled during the prenatal period. A 32-year-old pregnant woman was evaluated at our hospital following detection of increased nuchal translucency at 12 weeks and 5 days of...

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Detalles Bibliográficos
Autores principales: Kim, Kyoung-Bo, Ha, Jung-Sook, Shin, So-Jin, Kim, Chun Soo, Bae, Jin-Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Obstetrics and Gynecology; Korean Society of Contraception and Reproductive Health; Korean Society of Gynecologic Endocrinology; Korean Society of Gynecologic Endoscopy and Minimal Invasive Surgery; Korean Society of Maternal Fetal Medicine; Korean Society of Ultrasound in Obstetrics and Gynecology; Korean Urogynecologic Society 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124095/
https://www.ncbi.nlm.nih.gov/pubmed/25105107
http://dx.doi.org/10.5468/ogs.2014.57.4.318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124095/
https://www.ncbi.nlm.nih.gov/pubmed/25105107
http://dx.doi.org/10.5468/ogs.2014.57.4.318

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