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

Year Number of Results
1972 1
1973 2
1974 2
1975 4
1976 5
1977 3
1978 1
1979 4
1980 2
1981 7
1982 4
1983 9
1984 6
1985 6
1986 5
1987 4
1988 8
1989 4
1990 9
1991 6
1992 8
1993 6
1994 7
1995 8
1996 2
1997 19
1998 12
1999 9
2000 9
2001 18
2002 8
2003 3
2004 5
2005 3
2006 7
2007 3
2008 3
2009 1
2010 2
2012 1
2024 0

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224 results

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Page 1
The fragile X syndrome.
de Vries BB, Halley DJ, Oostra BA, Niermeijer MF. de Vries BB, et al. Among authors: niermeijer mf. J Med Genet. 1998 Jul;35(7):579-89. doi: 10.1136/jmg.35.7.579. J Med Genet. 1998. PMID: 9678703 Free PMC article. Review.
Kabuki syndrome: a review study of three hundred patients.
Wessels MW, Brooks AS, Hoogeboom J, Niermeijer MF, Willems PJ. Wessels MW, et al. Among authors: niermeijer mf. Clin Dysmorphol. 2002 Apr;11(2):95-102. doi: 10.1097/00019605-200204000-00004. Clin Dysmorphol. 2002. PMID: 12002156 Review.
Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: comparing questionnaire results with in-depth interviews. Rotterdam/Leiden Genetics Workgroup.
DudokdeWit AC, Tibben A, Duivenvoorden HJ, Niermeijer MF, Passchier J, Trijsburg RW. DudokdeWit AC, et al. Among authors: niermeijer mf. Am J Med Genet. 1998 Jan 6;75(1):62-74. doi: 10.1002/(sici)1096-8628(19980106)75:1<62::aid-ajmg14>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9450860 Review.
Prenatal diagnosis and genetic counseling of cystic fibrosis.
Niermeijer MF, Halley DJ, Kleijer WJ, Neijens HJ, Sinaasappel M. Niermeijer MF, et al. Acta Paediatr Scand Suppl. 1989;363:20-4. doi: 10.1111/apa.1989.78.s363.20. Acta Paediatr Scand Suppl. 1989. PMID: 2701920 Review.
224 results