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

Year Number of Results
1969 1
1974 1
1975 5
1976 1
1977 1
1978 1
1979 1
1985 3
1986 2
1987 1
1988 2
1989 1
1990 2
1992 5
1993 2
1994 3
1995 1
1996 2
1997 2
1998 4
1999 2
2001 4
2003 3
2004 2
2005 1
2006 4
2007 3
2009 1
2017 1
2020 1
2021 1
2022 1
2023 1
2024 0

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63 results

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Page 1
Familial occurrence of Hirschsprung's disease.
Russell MB, Russell CA, Fenger K, Niebuhr E. Russell MB, et al. Among authors: fenger k. Clin Genet. 1994 May;45(5):231-5. doi: 10.1111/j.1399-0004.1994.tb04147.x. Clin Genet. 1994. PMID: 8076407
Recurrence risk of myotonic dystrophy.
Fenger K, Hilden J. Fenger K, et al. Lancet. 1977 May 7;1(8019):1011. doi: 10.1016/s0140-6736(77)92315-7. Lancet. 1977. PMID: 67451 No abstract available.
4p16.3 haplotype modifying age at onset of Huntington disease.
Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L. Nørremølle A, et al. Among authors: fenger k. Clin Genet. 2009 Mar;75(3):244-50. doi: 10.1111/j.1399-0004.2008.01136.x. Clin Genet. 2009. PMID: 19250382
63 results