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

Year Number of Results
1962 1
1966 1
1968 1
1969 2
1970 5
1971 1
1973 4
1974 3
1976 2
1977 1
1978 1
1979 1
1980 2
1981 3
1982 3
1983 1
1984 5
1985 1
1986 2
1987 3
1988 6
1989 1
1990 4
1991 2
1992 4
1993 1
1994 3
1995 4
1996 2
1997 2
1998 1
2024 0

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73 results

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Page 1
Letter: Renpenning's syndrome.
Steele MW, Chorazy AL. Steele MW, et al. Lancet. 1974 Apr 20;1(7860):752-3. doi: 10.1016/s0140-6736(74)92978-x. Lancet. 1974. PMID: 4132492 No abstract available.
Research squeeze.
Steele MW. Steele MW. Nature. 1994 Sep 15;371(6494):194. doi: 10.1038/371194b0. Nature. 1994. PMID: 8078576 No abstract available.
Trisomy of chromosome 20.
Pan SF, Fatora SR, Haas JE, Steele MW. Pan SF, et al. Among authors: steele mw. Clin Genet. 1976 May;9(5):449-53. doi: 10.1111/j.1399-0004.1976.tb01595.x. Clin Genet. 1976. PMID: 1269166
A patient with a 47,XXY,5p- karyotype.
Palevsky S, Radfar N, Pan S, Steele MW. Palevsky S, et al. Among authors: steele mw. Clin Genet. 1979 Jul;16(1):43-6. doi: 10.1111/j.1399-0004.1979.tb00847.x. Clin Genet. 1979. PMID: 477014 No abstract available.
Terminal 2q deletion--a recognizable syndrome.
Wenger SL, Boone LY, Surti U, Steele MW. Wenger SL, et al. Among authors: steele mw. Clin Genet. 1997 Apr;51(4):290. doi: 10.1111/j.1399-0004.1997.tb02475.x. Clin Genet. 1997. PMID: 9184258 No abstract available.
Recurrence risk in 21q/21q translocation of Down syndrome.
Garver KL, Marchese SG, Steele MW, Ketterer DM. Garver KL, et al. Among authors: steele mw. J Pediatr. 1982 Feb;100(2):243-5. doi: 10.1016/s0022-3476(82)80646-x. J Pediatr. 1982. PMID: 6460094 No abstract available.
73 results