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

Year Number of Results
1968 1
1970 2
1971 4
1972 5
1973 6
1974 3
1975 12
1976 8
1977 3
1978 5
1979 2
1980 4
1981 4
1982 1
1983 3
1986 1
1987 2
1988 1
1989 3
1990 2
1991 2
1992 2
1994 4
1995 1
1996 4
1997 3
1998 1
1999 3
2000 4
2001 5
2002 2
2003 5
2004 2
2005 2
2006 3
2007 5
2008 3
2009 3
2010 1
2019 1
2024 0

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125 results

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Page 1
Fucosidosis type 2.
Kousseff BG, Beratis NG, Strauss L, Brill PW, Rosenfield RE, Kaplan B, Hirschhorn K. Kousseff BG, et al. Among authors: beratis ng. Pediatrics. 1976 Feb;57(2):205-13. Pediatrics. 1976. PMID: 814528
Prenatal diagnosis of renal anomalies.
Kaffe S, Rose JS, Godmilow L, Walker BA, Kerenyi T, Beratis N, Reyes P, Hirschhorn K. Kaffe S, et al. Among authors: beratis n. Am J Med Genet. 1977;1(2):241-51. doi: 10.1002/ajmg.1320010210. Am J Med Genet. 1977. PMID: 610432
47,XXY-48,XXXY-49,XXXXY mosaicism in a 4-year-old child.
Kardon NB, Beratis NG, Hsu LY, Moloshok RE, Hirschhorn K. Kardon NB, et al. Among authors: beratis ng. Am J Dis Child. 1971 Aug;122(2):160-2. Am J Dis Child. 1971. PMID: 5564159 No abstract available.
Trisomy 18.
Kardon N, Hsu LY, Beratis N, Hirschhorn K. Kardon N, et al. Among authors: beratis n. Lancet. 1970 Oct 10;2(7676):782. doi: 10.1016/s0140-6736(70)90272-2. Lancet. 1970. PMID: 4196013 No abstract available.
Sanfilippo disease in Greece.
Beratis NG, Sklower SL, Wilbur L, Matalon R. Beratis NG, et al. Clin Genet. 1986 Feb;29(2):129-32. doi: 10.1111/j.1399-0004.1986.tb01235.x. Clin Genet. 1986. PMID: 3082543
Polymorphism of human alpha fucosidase.
Turner BM, Turner VS, Beratis NG, Hirschhorn K. Turner BM, et al. Among authors: beratis ng. Am J Hum Genet. 1975 Sep;27(5):651-61. Am J Hum Genet. 1975. PMID: 1163537 Free PMC article.
125 results