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Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?
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- Bruder, CEG (author)
- Karolinska Institutet
- Ichimura, K (author)
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- Blennow, E (author)
- Karolinska Institutet
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- Ikeuchi, T (author)
- Yamaguchi, T (author)
- Yuasa, Y (author)
- Collins, VP (author)
- Dumanski, JP (author)
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- (creator_code:org_t)
- 1999
- 1999
- English.
- In: Genes, chromosomes & cancer. - 1045-2257. ; 25:2, s. 184-190
- Journal article (peer-reviewed)
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- Blennow, E
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- Yuasa, Y
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- Dumanski, JP
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