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

Year Number of Results
1984 2
1985 1
1986 2
1987 2
1988 1
1989 2
1990 3
1992 5
1993 12
1994 11
1995 12
1996 10
1997 7
1998 5
1999 8
2000 7
2001 1
2024 0

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91 results

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Page 1
Molecular analysis of the 18q- syndrome--and correlation with phenotype.
Kline AD, White ME, Wapner R, Rojas K, Biesecker LG, Kamholz J, Zackai EH, Muenke M, Scott CI Jr, Overhauser J. Kline AD, et al. Among authors: overhauser j. Am J Hum Genet. 1993 May;52(5):895-906. Am J Hum Genet. 1993. PMID: 8488839 Free PMC article. Review.
Neuropsychiatry of 18q- syndrome.
Mahr RN, Moberg PJ, Overhauser J, Strathdee G, Kamholz J, Loevner LA, Campbell H, Zackai EH, Reber ME, Mozley DP, Brown L, Turetsky BI, Shapiro RM. Mahr RN, et al. Among authors: overhauser j. Am J Med Genet. 1996 Apr 9;67(2):172-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<172::AID-AJMG7>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8723044
Molecular analysis of 18q deletions.
Overhauser J. Overhauser J. Prog Clin Biol Res. 1993;384:175-85. Prog Clin Biol Res. 1993. PMID: 8115401 Review. No abstract available.
Somatic cell hybrid deletion map of human chromosome 18.
Kline AD, Rojas K, Mewar R, Moshinsky D, Overhauser J. Kline AD, et al. Among authors: overhauser j. Genomics. 1992 May;13(1):1-6. doi: 10.1016/0888-7543(92)90193-v. Genomics. 1992. PMID: 1577474
5p14 deletion associated with microcephaly and seizures.
Johnson EI, Marinescu RC, Punnett HH, Tenenholz B, Overhauser J. Johnson EI, et al. Among authors: overhauser j. J Med Genet. 2000 Feb;37(2):125-7. doi: 10.1136/jmg.37.2.125. J Med Genet. 2000. PMID: 10662813 Free PMC article.
91 results