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Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. [electronic resource] by
- Vogt, Julia
- Mussotter, Tanja
- Bengesser, Kathrin
- Claes, Kathleen
- Högel, Josef
- Chuzhanova, Nadia
- Fu, Chuanhua
- van den Ende, Jenneke
- Mautner, Victor-Felix
- Cooper, David N
- Messiaen, Ludwine
- Kehrer-Sawatzki, Hildegard
Producer: 20130304
In:
Human mutation vol. 33
Availability: No items available.
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