✦ LIBER ✦

Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs

✍ Scribed by Kmita, Marie; Fraudeau, Nadine; Hérault, Yann; Duboule, Denis

Book ID: 109890666
Publisher: Nature Publishing Group
Year: 2002
Tongue: English
Weight: 389 KB
Volume: 420
Category: Article
ISSN: 0028-0836
DOI: 10.1038/nature01189

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intragenic deletions and duplications of

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

✍ Haverfield, Eden V; Whited, Amanda J; Petras, Kristin S; Dobyns, William B; Das, 📂 Article 📅 2008 🏛 Nature Publishing Group 🌐 English ⚖ 135 KB

Intronic deletion and duplication proxim

Intronic deletion and duplication proximal of the EXT1 gene: A novel causative mechanism for multiple osteochondromas

✍ Waaijer, Cathelijn J. F.; Winter, Marcel G. T.; Reijnders, Christianne M. A.; de 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 391 KB

Recurrent inversion with concomitant del

Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A

✍ Christiane Mühle; Martin Zenker; Nadia Chuzhanova; Holm Schneider 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 369 KB

Recurrent int22h-related inversions in the coagulation factor VIII gene (F8) are the most common cause of severe hemophilia A. Such inversions have repeatedly been hypothesized to be associated with concomitant deletions that are responsible for an increased risk of immune responses against therapeu

A Suggested Control Gene Mechanism for t

✍ C. J. Watson, W. Runge, L. Taddeini, Irene Bossenmaier and Ruth Cardinal 📂 Article 📅 1964 🏛 National Academy of Sciences 🌐 English ⚖ 318 KB

Pericentric inversion, inv(9) (p22 q32),

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1

✍ J. F. Mattei; M. G. Mattei; J. P. Ardissone; H. Taramasco; F. Giraud 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 521 KB

The 3′ breakpoint of the Yunnanese (Aγδβ

The 3′ breakpoint of the Yunnanese (Aγδβ)0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of theGγ-globin gene

✍ Xue-Qing Zhang; J.-W. Zhang 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 248 KB