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Severe phenotype of...
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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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LIBRIS-ID:oai:prod.swepub.kib.ki.se:1938005
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http://kipublications.ki.se/Default.aspx?queryparsed=id:1938005URI
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
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Ichimura, K
(author)
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Blennow, EKarolinska Institutet
(author)
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Ikeuchi, T
(author)
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Yamaguchi, T
(author)
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Yuasa, Y
(author)
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Collins, VP
(author)
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Dumanski, JP
(author)
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Karolinska Institutet
(creator_code:org_t)
Related titles
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In:Genes, chromosomes & cancer25:2, s. 184-1901045-2257
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