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Results by year

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

Year Number of Results
1993 2
1995 2
1998 1
1999 3
2000 1
2001 2
2002 1
2005 1
2009 1
2010 1
2018 1
2019 1
2024 0

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16 results

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Page 1
Phenotypic variability of Cat-Eye syndrome.
Berends MJ, Tan-Sindhunata G, Leegte B, van Essen AJ. Berends MJ, et al. Among authors: leegte b. Genet Couns. 2001;12(1):23-34. Genet Couns. 2001. PMID: 11332976 Review.
Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.
Leegte B, van der Hout AH, Deffenbaugh AM, Bakker MK, Mulder IM, ten Berge A, Leenders EP, Wesseling J, de Hullu J, Hoogerbrugge N, Ligtenberg MJ, Ardern-Jones A, Bancroft E, Salmon A, Barwell J, Eeles R, Oosterwijk JC. Leegte B, et al. J Med Genet. 2005 Mar;42(3):e20. doi: 10.1136/jmg.2004.027243. J Med Genet. 2005. PMID: 15744030 Free PMC article. Review. No abstract available.
Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.
Verheij JB, Bouman K, van Lingen RA, van Lookeren Campagne JG, Leegte B, van der Veen AY, Hofstra RM, Buys CH, van Essen AJ. Verheij JB, et al. Among authors: leegte b. Am J Med Genet. 1999 Sep 10;86(2):168-73. doi: 10.1002/(sici)1096-8628(19990910)86:2<168::aid-ajmg16>;2-q. Am J Med Genet. 1999. PMID: 10449655 Review.
Bilateral split hand/foot malformation and inv(7)(p22q21.3).
Cobben JM, Verheij JB, Eisma WH, Robinson PH, Zwierstra RP, Leegte B, Castedo S. Cobben JM, et al. Among authors: leegte b. J Med Genet. 1995 May;32(5):375-8. doi: 10.1136/jmg.32.5.375. J Med Genet. 1995. PMID: 7616545 Free PMC article.
Time to stop ovarian cancer screening in BRCA1/2 mutation carriers?
van der Velde NM, Mourits MJ, Arts HJ, de Vries J, Leegte BK, Dijkhuis G, Oosterwijk JC, de Bock GH. van der Velde NM, et al. Among authors: leegte bk. Int J Cancer. 2009 Feb 15;124(4):919-23. doi: 10.1002/ijc.24038. Int J Cancer. 2009. PMID: 19035463 Free article.
16 results