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Results by year

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

Year Number of Results
1988 4
1989 1
1990 1
1992 1
1994 1
1995 1
1998 5
1999 5
2000 12
2001 6
2002 10
2003 1
2004 6
2005 5
2024 0

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PubMed (OMIM) for id: 8063

59 results

Results by year

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Page 1
A proportion of patients with lymphoma may harbor mutations of the perforin gene.
Clementi R, Locatelli F, Dupré L, Garaventa A, Emmi L, Bregni M, Cefalo G, Moretta A, Danesino C, Comis M, Pession A, Ramenghi U, Maccario R, Aricò M, Roncarolo MG. Clementi R, et al. Blood. 2005 Jun 1;105(11):4424-8. doi: 10.1182/blood-2004-04-1477. Epub 2005 Feb 22. Blood. 2005. PMID: 15728124 Free article.
Autoimmune lymphoproliferative syndrome and perforin.
Rieux-Laucat F, Le Deist F, De Saint Basile G. Rieux-Laucat F, et al. N Engl J Med. 2005 Jan 20;352(3):306-7; author reply 306-7. doi: 10.1056/NEJM200501203520319. N Engl J Med. 2005. PMID: 15659737 No abstract available.
Homozygosis for (12) CA repeats in the first intron of the human IFN-gamma gene is significantly associated with the risk of aplastic anaemia in Caucasian population.
Dufour C, Capasso M, Svahn J, Marrone A, Haupt R, Bacigalupo A, Giordani L, Longoni D, Pillon M, Pistorio A, Di Michele P, Iori AP, Pongiglione C, Lanciotti M, Iolascon A; Associazione Italiana di Emato-Oncologia Pediatrica (AIEOP); Department of Hematology, Ospedale S. Martino, Genoa, Italy. Dufour C, et al. Br J Haematol. 2004 Sep;126(5):682-5. doi: 10.1111/j.1365-2141.2004.05102.x. Br J Haematol. 2004. PMID: 15327519 Free article.
59 results