✦ LIBER ✦

Beckwith–Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a “de novo” pericentric inversion of chromosome Y

✍ Scribed by Alicia Delicado; Pablo Lapunzina; María Palomares; Maria Antonia Molina; Enrique Galán; Isidora López Pajares

Book ID: 116432771
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 177 KB
Volume: 48
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2005.01.017

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Co-occurrence of 4p16.3 deletions with b

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype

✍ Sarah T. South; Heidi Whitby; Teresa Maxwell; Emily Aston; Arthur R. Brothman; J 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 183 KB 👁 2 views