id:"swepub:oai:prod.swepub.kib.ki.se:1938005"
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- Bruder, CEGKarolinska Institutet (author)
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?
- Article/chapterEnglish1999
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- 1999
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:1938005
- http://kipublications.ki.se/Default.aspx?queryparsed=id:1938005URI
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- Language:English
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- Ichimura, K (author)
- Blennow, EKarolinska Institutet (author)
- Ikeuchi, T (author)
- Yamaguchi, T (author)
- Yuasa, Y (author)
- Collins, VP (author)
- Dumanski, JP (author)
- Karolinska Institutet (creator_code:org_t)
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- In:Genes, chromosomes & cancer25:2, s. 184-1901045-2257
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