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- Vogt, Julia
- Cooper, David N 7
- Mautner, Viktor Felix 7
- Kehrer-Sawatzki, Hildegard 6
- Kluwe, Lan 6
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9 Einträge gefunden
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Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1
- Thomas, Christian
- Knerlich-Lukoschus, Friederike
- Reinhard, Harald
- Johann, Pascal D
- Sturm, Dominik
- Sahm, Felix
- Bens, Susanne
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Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination
- Bengesser, Kathrin
- Vogt, Julia
- Mussotter, Tanja
- Mautner, Victor-Felix
- Messiaen, Ludwine
- Cooper, David N
- Kehrer-Sawatzki, Hildegard
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Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletions.
- Kehrer-Sawatzki, Hildegard
- Vogt, Julia
- Mußotter, Tanja
- Kluwe, Lan
- Cooper, David N
- Mautner, Viktor Felix
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Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/-) stem cells.
- Roehl, Angelika C
- Mussotter, Tanja
- Cooper, David N
- Kluwe, Lan
- Wimmer, Katharina
- Högel, Josef
- Zetzmann, Marion
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Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions.
- Kluwe, Lan
- Nguyen, Rosa
- Vogt, Julia
- Bengesser, Kathrin
- Mussotter, Tanja
- Friedrich, Reinhard
- Jett, Kimberly
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Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder.
- Vogt, Julia
- Mussotter, Tanja
- Bengesser, Kathrin
- Claes, Kathleen
- Högel, Josef
- Chuzhanova, Nadia
- Fu, Chuanhua
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Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reports.
- Vogt, Julia
- Nguyen, Rosa
- Kluwe, Lan
- Schuhmann, Martin
- Roehl, Angelika C
- Mußotter, Tanja
- Cooper, David N
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