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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1928 1
1954 1
1961 5
1962 2
1964 1
1967 1
1968 1
1969 2
1970 3
1971 4
1973 1
1976 2
1978 1
1979 3
1981 1
1982 1
1984 1
1986 2
1987 2
1988 4
1989 5
1990 5
1991 6
1992 3
1993 4
1994 7
1995 3
1996 3
1997 2
1998 3
1999 3
2000 6
2001 4
2002 2
2003 3
2004 3
2005 1
2006 1
2007 5
2009 3
2010 1
2012 1
2015 1
2016 1
2018 2
2024 0

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Publication date

PubMed (cited) for id: 193300

115 results

Results by year

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Page 1
Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease.
Lenglet M, Robriquet F, Schwarz K, Camps C, Couturier A, Hoogewijs D, Buffet A, Knight SJL, Gad S, Couvé S, Chesnel F, Pacault M, Lindenbaum P, Job S, Dumont S, Besnard T, Cornec M, Dreau H, Pentony M, Kvikstad E, Deveaux S, Burnichon N, Ferlicot S, Vilaine M, Mazzella JM, Airaud F, Garrec C, Heidet L, Irtan S, Mantadakis E, Bouchireb K, Debatin KM, Redon R, Bezieau S, Bressac-de Paillerets B, Teh BT, Girodon F, Randi ML, Putti MC, Bours V, Van Wijk R, Göthert JR, Kattamis A, Janin N, Bento C, Taylor JC, Arlot-Bonnemains Y, Richard S, Gimenez-Roqueplo AP, Cario H, Gardie B. Lenglet M, et al. 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.
Genetic analysis of von Hippel-Lindau disease.
Nordstrom-O'Brien M, van der Luijt RB, van Rooijen E, van den Ouweland AM, Majoor-Krakauer DF, Lolkema MP, van Brussel A, Voest EE, Giles RH. Nordstrom-O'Brien M, et al. Hum Mutat. 2010 May;31(5):521-37. doi: 10.1002/humu.21219. Hum Mutat. 2010. PMID: 20151405
Genotype-phenotype correlations in VHL exon deletions.
McNeill A, Rattenberry E, Barber R, Killick P, MacDonald F, Maher ER. McNeill A, et al. Am J Med Genet A. 2009 Oct;149A(10):2147-51. doi: 10.1002/ajmg.a.33023. Am J Med Genet A. 2009. PMID: 19764026
115 results