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Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1)

✍ Scribed by Chen, Chih-Ping; Chang, Shing-Jyh; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yu-Ting; Su, Jun-Wei; Chen, Wen-Lin; Wang, Wayseen


Book ID
120171420
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
716 KB
Volume
521
Category
Article
ISSN
0378-1119

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✍ Andreas Tzschach; Ines Krause-Plonka; Corinna Menzel; Andreas Knoblauch; Holger 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 104 KB 👁 2 views

## Abstract Interstitial deletions of 10q are rare, and only one patient with a deletion confined to chromosome band 10q22 has been reported so far. We report on a 2 6/12‐year‐old girl with a constitutional interstitial deletion of one homologue of 10q [karyotype: 46,XX,del(10)(q22.2q22.3)de novo].