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

Year Number of Results
1976 3
1977 2
1982 1
1983 1
1985 2
1986 2
1987 6
1988 1
1989 1
1990 2
1991 3
1992 2
1994 2
1995 6
1996 9
1997 1
1998 3
1999 9
2000 5
2001 3
2002 3
2003 3
2004 2
2005 5
2006 3
2007 4
2008 4
2009 1
2011 1
2019 1
2024 0

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91 results

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Page 1
Cystathionine beta-synthase mutations in homocystinuria.
Kraus JP, Janosík M, Kozich V, Mandell R, Shih V, Sperandeo MP, Sebastio G, de Franchis R, Andria G, Kluijtmans LA, Blom H, Boers GH, Gordon RB, Kamoun P, Tsai MY, Kruger WD, Koch HG, Ohura T, Gaustadnes M. Kraus JP, et al. Among authors: sebastio g. Hum Mutat. 1999;13(5):362-75. doi: 10.1002/(SICI)1098-1004(1999)13:5<362::AID-HUMU4>3.0.CO;2-K. Hum Mutat. 1999. PMID: 10338090 Review.
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
Garavelli L, Zollino M, Mainardi PC, Gurrieri F, Rivieri F, Soli F, Verri R, Albertini E, Favaron E, Zignani M, Orteschi D, Bianchi P, Faravelli F, Forzano F, Seri M, Wischmeijer A, Turchetti D, Pompilii E, Gnoli M, Cocchi G, Mazzanti L, Bergamaschi R, De Brasi D, Sperandeo MP, Mari F, Uliana V, Mostardini R, Cecconi M, Grasso M, Sassi S, Sebastio G, Renieri A, Silengo M, Bernasconi S, Wakamatsu N, Neri G. Garavelli L, et al. Among authors: sebastio g. Am J Med Genet A. 2009 Mar;149A(3):417-26. doi: 10.1002/ajmg.a.32693. Am J Med Genet A. 2009. PMID: 19215041 Review.
Characterization of phenylketonuria alleles in the Italian population.
Dianzani I, Giannattasio S, de Sanctis L, Alliaudi C, Lattanzio P, Dionisi Vici C, Burlina A, Burroni M, Sebastio G, Carnevale F, et al. Dianzani I, et al. Among authors: sebastio g. Eur J Hum Genet. 1995;3(5):294-302. doi: 10.1159/000472313. Eur J Hum Genet. 1995. PMID: 8556304
91 results