Advanced search
1 file | 397.12 KB

Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

(2012) HUMAN MUTATION. 33(11). p.1599-1609
Author
Organization
Keywords
mosaicism, hotspot, NF1 microdeletions, nonallelic homologous recombination, HUMAN INHERITED DISEASE, COPY-NUMBER-VARIATION, SCAFFOLD/MATRIX ATTACHMENT REGIONS, BREAK-INDUCED REPLICATION, NEUROFIBROMATOSIS TYPE-1, MEIOTIC RECOMBINATION, GENE CONVERSION, GLOBIN GENES, DNA, DELETIONS

Downloads

  • (...).pdf
    • full text
    • |
    • UGent only
    • |
    • PDF
    • |
    • 397.12 KB

Citation

Please use this url to cite or link to this publication:

Chicago
Vogt, Julia, Tanja Mussotter, Kathrin Bengesser, Kathleen Claes, Josef Högel, Nadia Chuzhanova, Chuanhua Fu, et al. 2012. “Identification of Recurrent Type-2 NF1 Microdeletions Reveals a Mitotic Nonallelic Homologous Recombination Hotspot Underlying a Human Genomic Disorder.” Human Mutation 33 (11): 1599–1609.
APA
Vogt, J., Mussotter, T., Bengesser, K., Claes, K., Högel, J., Chuzhanova, N., Fu, C., et al. (2012). Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. HUMAN MUTATION, 33(11), 1599–1609.
Vancouver
1.
Vogt J, Mussotter T, Bengesser K, Claes K, Högel J, Chuzhanova N, et al. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. HUMAN MUTATION. 2012;33(11):1599–609.
MLA
Vogt, Julia, Tanja Mussotter, Kathrin Bengesser, et al. “Identification of Recurrent Type-2 NF1 Microdeletions Reveals a Mitotic Nonallelic Homologous Recombination Hotspot Underlying a Human Genomic Disorder.” HUMAN MUTATION 33.11 (2012): 1599–1609. Print.
@article{3158342,
  author       = {Vogt, Julia and Mussotter, Tanja and Bengesser, Kathrin and Claes, Kathleen and H{\"o}gel, Josef and Chuzhanova, Nadia and Fu, Chuanhua and van den Ende, Jenneke and Mautner, Victor-Felix and Cooper, David N and Messiaen, Ludwine and Kehrer-Sawatzkil, Hildegard},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {11},
  pages        = {1599--1609},
  title        = {Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder},
  url          = {http://dx.doi.org/10.1002/humu.22171},
  volume       = {33},
  year         = {2012},
}

Altmetric
View in Altmetric
Web of Science
Times cited: