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Results by year

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

Year Number of Results
1964 1
1967 1
1968 2
1969 1
1970 1
1971 2
1973 2
1974 1
1975 8
1976 4
1977 2
1978 1
1979 2
1980 3
1981 2
1982 1
1983 2
1984 2
1985 4
1986 2
1987 5
1988 3
1989 1
1990 3
1991 1
1992 6
1994 6
1995 6
1996 2
1997 4
1998 5
1999 5
2000 3
2001 1
2003 1
2004 4
2007 1
2009 1
2024 0

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Search Results

102 results

Results by year

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Page 1
Mesomelic skeletal dysplasias.
Kaitila I, Leisti JT, Rimoin DL. Kaitila I, et al. Among authors: leisti jt. Clin Orthop Relat Res. 1976 Jan-Feb;(114):94-106. Clin Orthop Relat Res. 1976. PMID: 1261139
The Floating-Harbor syndrome.
Leisti J, Hollister DW, Rimoin DL. Leisti J, et al. Birth Defects Orig Artic Ser. 1975;11(5):305. Birth Defects Orig Artic Ser. 1975. PMID: 1218224 No abstract available.
Muscle-eye-brain disease (MEB).
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T, Ketonen L, Leisti J. Santavuori P, et al. Among authors: leisti j. Brain Dev. 1989;11(3):147-53. doi: 10.1016/s0387-7604(89)80088-9. Brain Dev. 1989. PMID: 2751061
Partial trisomy 21.
Aula P, Leisti J, von Koskull H. Aula P, et al. Among authors: leisti j. Clin Genet. 1973;4(3):241-51. doi: 10.1111/j.1399-0004.1973.tb01149.x. Clin Genet. 1973. PMID: 4128808 No abstract available.
Dysosteosclerosis.
Leisti J, Kaitila I, Lachman RS, Asch MJ, Rimoin DL. Leisti J, et al. Birth Defects Orig Artic Ser. 1975;11(6):349-51. Birth Defects Orig Artic Ser. 1975. PMID: 1201343 No abstract available.
[XYY-syndrome].
Aula P, Leisti J, Hirvonen J, Sallas O. Aula P, et al. Among authors: leisti j. Duodecim. 1969;85(19):1198-204. Duodecim. 1969. PMID: 5371708 Finnish. No abstract available.
Muscle-eye-brain disease and Walker-Warburg syndrome.
Santavuori P, Pihko H, Sainio K, Lappi M, Somer H, Haltia M, Raitta C, Ketonen L, Leisti J. Santavuori P, et al. Among authors: leisti j. Am J Med Genet. 1990 Jul;36(3):371-4. doi: 10.1002/ajmg.1320360334. Am J Med Genet. 1990. PMID: 2363444 No abstract available.
Identification of the familial cylindromatosis tumour-suppressor gene.
Bignell GR, Warren W, Seal S, Takahashi M, Rapley E, Barfoot R, Green H, Brown C, Biggs PJ, Lakhani SR, Jones C, Hansen J, Blair E, Hofmann B, Siebert R, Turner G, Evans DG, Schrander-Stumpel C, Beemer FA, van Den Ouweland A, Halley D, Delpech B, Cleveland MG, Leigh I, Leisti J, Rasmussen S. Bignell GR, et al. Among authors: leisti j. Nat Genet. 2000 Jun;25(2):160-5. doi: 10.1038/76006. Nat Genet. 2000. PMID: 10835629
102 results