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Year | Number of Results |
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2005 | 1 |
2018 | 1 |
2024 | 0 |
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Page 1
Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease.
Blood. 2018 Aug 2;132(5):469-483. doi: 10.1182/blood-2018-03-838235. Epub 2018 Jun 11.
Blood. 2018.
PMID: 29891534
Free article.
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis.
Cario H, Schwarz K, Jorch N, Kyank U, Petrides PE, Schneider DT, Uhle R, Debatin KM, Kohne E.
Cario H, et al.
Haematologica. 2005 Jan;90(1):19-24.
Haematologica. 2005.
PMID: 15642664
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