Mosaic Type-1 NF1 Microdeletions as a Cause of Both Generalized and Segmental Neurofibromatosis Type-1 (NF1)

Erstveröffentlichung

2011

Authors

Messiaen, Ludwine

Vogt, Julia

Bengesser, Kathrin

Fu, Chuanhua

Mikhail, Fady

et al.

Wissenschaftlicher Artikel

Published in

Human mutation ; 32 (2011), 2. - S. 213-219. - ISSN 1059-7794. - eISSN 1098-1004

Link to publication

https://dx.doi.org/10.1002/humu.21418

Institutions

UKU. Institut für Humangenetik

Subject headings

[Free subject headings]: neurofibromatosis type 1 | NF1 | microdeletion | recombination hotspots | mosaicism | NONALLELIC HOMOLOGOUS RECOMBINATION | LOW-COPY REPEATS | MOLECULAR CHARACTERIZATION | SOMATIC MOSAICISM | GENE | DELETIONS | 17Q11.2 | MUTATION | HOTSPOTS | REGION
[DDC subject group]: DDC 570 / Life sciences

Metadata

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