A Novel Third Type of Recurrent NF1 Microdeletion Mediated by Nonallelic Homologous Recombination between LRRC37B-Containing Low-Copy Repeats in 17q11.2

Erstveröffentlichung

2010

Authors

Bengesser, Kathrin

Cooper, David N.

Steinmann, Katherina

Kluwe, Lan

Chuzhanova, Nadia A.

et al.

Wissenschaftlicher Artikel

Published in

Human mutation ; 31 (2010), 6. - S. 742-751. - ISSN 1059-7794. - eISSN 1098-1004

Link to publication

https://dx.doi.org/10.1002/humu.21254

Institutions

UKU. Institut für Humangenetik

Publisher

Hoboken, NJ : Wiley

ISSN

1059-7794

eISSN

1098-1004

Subject headings

[Free subject headings]: genomic disorders | NAHR | microdeletions | neurofibromatosis type-1 | NF1 | nonallelic homologous recombination | 17q11.2 | B DNA CONFORMATIONS | HUMAN INHERITED DISEASE | HUMAN GENOME | 17Q21.31 MICRODUPLICATION | MITOTIC RECOMBINATION | COMMON INVERSION | HUMAN LINEAGE | GENE CONTENT | REGION
[DDC subject group]: DDC 570 / Life sciences

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