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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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Autori principali: Kim, Kyoung-Bo, Ha, Jung-Sook, Shin, So-Jin, Kim, Chun Soo, Bae, Jin-Gon
Natura: Artigo
Lingua:Inglês
Pubblicazione: 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
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4124095/
https://ncbi.nlm.nih.gov/pubmed/25105107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5468/ogs.2014.57.4.318
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