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- Kluwe, Lan
- Mautner, Viktor Felix 24
- Cooper, David N 6
- Friedrich, Reinhard 6
- Kehrer-Sawatzki, Hildegard 5
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26 Einträge gefunden
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Large intragenic deletions of the NF2 gene: breakpoints and associated phenotypes.
2010 - Forschungsinformationssystem des UKE -
Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burden.
2010 - Forschungsinformationssystem des UKE -
A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2.
- Bengesser, Kathrin
- Cooper, David N
- Steinmann, Katharina
- Kluwe, Lan
- Chuzhanova, Nadia A
- Wimmer, Katharina
- Tatagiba, Marcos
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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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Ral overactivation in malignant peripheral nerve sheath tumors.
- Vidya, Bodempudi
- Yamoutpoor, Farnaz
- Pan, Weihong
- Dudek, Arkadiusz Z
- Esfandyari, Tuba
- Piedra, Mark
- Babovick-Vuksanovic, Dusica
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The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas.
- Upadhyaya, Meena
- Spurlock, Gill
- Kluwe, Lan
- Chuzhanova, Nadia
- Bennett, Emma
- Thomas, Nick
- Guha, Abhijit
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Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis.
2008 - Forschungsinformationssystem des UKE -
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Germline and somatic NF1 gene mutations in plexiform neurofibromas.
- Upadhyaya, Meena
- Spurlock, Gill
- Monem, Bisma
- Thomas, Nick
- Friedrich, Reinhard
- Kluwe, Lan
- Mautner, Viktor Felix
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Assessment of benign tumor burden by whole-body MRI in patients with neurofibromatosis 1.
- Mautner, Viktor Felix
- Asuagbor, Florence A
- Dombi, Eva
- Fünsterer, Carsten
- Kluwe, Lan
- Wenzel, Ralf
- Widemann, Brigitte C
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Correlation of nonsense and frameshift mutations with severity of retinal abnormalities in neurofibromatosis 2.
2008 - Forschungsinformationssystem des UKE