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De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male

✍ Scribed by Iman Salahshourifar; Mohammad Ali Sedighi Gilani; Ahmad Vosough; Tayebeh Tavakolzadeh; Masoumeh Tahsili; Zahra Mansori; Hamideh Karimi; Mehdi Totonchi; Hamid Gourabi

Book ID: 105732792
Publisher: Springer-Verlag
Year: 2007
Tongue: English
Weight: 69 KB
Volume: 48
Category: Article
ISSN: 1234-1983
DOI: 10.1007/bf03194664

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MOLECULAR ANALYSIS BY FLUORESCENCE IN SI

MOLECULAR ANALYSIS BY FLUORESCENCE IN SITU HYBRIDIZATION OF A PRENATALLY DETECTED DE NOVO COMPLEX CHROMOSOMAL REARRANGEMENT t(2q;3p;4q;13q)

✍ S. MERCIER; F. FELLMANN; J. CATTIN; J. L. BRESSON 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 783 KB

We report one case of de novo complex chromosomal rearrangement (CCR) t(2q;3p;4q;13q) with at least five chromosomal breakpoints. This CCR was detected prenatally at 22 weeks of gestation, when mild echographic indications were disclosed during a routine examination in a female with no family histor