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- Högel, Josef
- Cooper, David N 5
- Mautner, Viktor Felix 5
- Kluwe, Lan 4
- Kehrer-Sawatzki, Hildegard 3
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9 Einträge gefunden
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De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- Hübers, Annemarie
- Just, Walter
- Rosenbohm, Angela
- Müller, Kathrin
- Marroquin, Nicolai
- Goebel, Ingrid
- Högel, Josef
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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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Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions.
- Mußotter, Tanja
- Kluwe, Lan
- Högel, Josef
- Nguyen, Rosa
- Cooper, David N
- Mautner, Viktor Felix
- Kehrer-Sawatzki, Hildegard
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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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Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions?
- Roehl, Angelika C
- Cooper, David N
- Kluwe, Lan
- Helbrich, Andreas
- Wimmer, Katharina
- Högel, Josef
- Mautner, Viktor Felix
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