✦ LIBER ✦

605: Clinical utility of chromosomal microarray analysis in prenatal diagnosis in a diverse urban center

✍ Scribed by Spencer, Brianna; Klugman, Susan; Suskin, Barrie; Bajaj, Komal; Goldwaser, Tamar; Powers, Judith; Reichling, Julie; Dolan, Siobhan; Merkatz, Irwin

Book ID: 119185724
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 199 KB
Volume: 208
Category: Article
ISSN: 1097-6868
DOI: 10.1016/j.ajog.2012.10.771

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Clinical utility of chromosomal microarr

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

✍ Lluís Armengol; Julián Nevado; Clara Serra-Juhé; Alberto Plaja; Carmen Mediano; 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 245 KB

The clinical utility and indications of

The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis

✍ Alesi, V; Bertoli, M; Sinibaldi, L; Novelli, A 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 59 KB

Authors' response to: The clinical utili

Authors' response to: The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis

✍ Lee, C-N; Lin, S-Y; Shih, J-C; Su, Y-N 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 41 KB

Prenatal diagnosis of chromosomal abnorm

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis

✍ Mademont-Soler, I.; Morales, C.; Soler, A.; MartÍnez-Crespo, J. M.; Shen, Y.; Ma 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 188 KB

A prospective study of the clinical util

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors

✍ Brady, Paul Daniel; Delle Chiaie, Barbara; Christenhusz, Gabrielle; Dierickx, Kr 📂 Article 📅 2013 🏛 Nature Publishing Group 🌐 English ⚖ 732 KB

An exon 1 deletion in OTC identified usi

An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: Implications for the prenatal diagnosis of ornithine transcarbamylase deficiency

✍ Fabiola Quintero-Rivera; Joshua L. Deignan; Jane Peredo; Wayne W. Grody; Barbara 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 376 KB