Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination

Erstveröffentlichung

2007

Authors

Steinmann, Katharina

Cooper, David N.

Kluwe, Lan

Chuzhanova, Nadia A.

Senger, Cornelia

et al.

Wissenschaftlicher Artikel

Published in

American Journal of Human Genetics ; 81 (2007), 6. - S. 1201-1220. - ISSN 0002-9297. - eISSN 1537-6605

Link to publication

https://dx.doi.org/10.1086/522089

Institutions

UKU. Institut für Humangenetik

Subject headings

[Free subject headings]: TUMOR-SUPPRESSOR REGION | HUMAN INHERITED DISEASE | B DNA CONFORMATIONS | NEUROFIBROMATOSIS TYPE-1 | INTRACHROMOSOMAL RECOMBINATION | GENOMIC REARRANGEMENTS | MEIOTIC RECOMBINATION | V(D)J RECOMBINATION | MOLECULAR ANALYSIS | SOMATIC MOSAICISM
[DDC subject group]: DDC 570 / Life sciences

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