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

Erstveröffentlichung
2011Authors
Messiaen, Ludwine
Vogt, Julia
Bengesser, Kathrin
Fu, Chuanhua
Mikhail, Fady
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.21418Institutions
UKU. Institut für HumangenetikSubject 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