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Results by year

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

Year Number of Results
1960 1
1964 1
1965 1
1966 2
1967 1
1968 1
1969 2
1971 2
1972 2
1973 1
1975 2
1977 1
1979 1
1983 3
1984 2
1985 1
1986 2
1987 5
1988 1
1989 1
1990 1
1991 1
1992 1
1993 2
1994 7
1995 6
1996 4
1997 11
1998 10
1999 6
2000 7
2001 8
2002 1
2003 1
2004 2
2005 1
2024 0

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PubMed (OMIM) for id: 61231

102 results

Results by year

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Page 1
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome.
Witsch-Baumgartner M, Gruber M, Kraft HG, Rossi M, Clayton P, Giros M, Haas D, Kelley RI, Krajewska-Walasek M, Utermann G. Witsch-Baumgartner M, et al. J Med Genet. 2004 Aug;41(8):577-84. doi: 10.1136/jmg.2004.018085. J Med Genet. 2004. PMID: 15286151 Free PMC article.
Smith-Lemli-Opitz syndrome: new mutation with a mild phenotype.
Prasad C, Marles S, Prasad AN, Nikkel S, Longstaffe S, Peabody D, Eng B, Wright S, Waye JS, Nowaczyk MJ. Prasad C, et al. Am J Med Genet. 2002 Feb 15;108(1):64-8. doi: 10.1002/ajmg.10211. Am J Med Genet. 2002. PMID: 11857552
102 results