Leegte BK - Search Results

1

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.

2

Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age.

van der Kolk DM, de Bock GH, Leegte BK, Schaapveld M, Mourits MJ, de Vries J, van der Hout AH, Oosterwijk JC. van der Kolk DM, et al. Among authors: leegte bk. Breast Cancer Res Treat. 2010 Dec;124(3):643-51. doi: 10.1007/s10549-010-0805-3. Epub 2010 Mar 4. Breast Cancer Res Treat. 2010. PMID: 20204502

3

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.

4

Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.

van Essen AJ, Schoots CJ, van Lingen RA, Mourits MJ, Tuerlings JH, Leegte B. van Essen AJ, et al. Am J Med Genet. 1993 Aug 1;47(1):85-8. doi: 10.1002/ajmg.1320470117. Am J Med Genet. 1993. PMID: 8368259 Review.

5

Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].

Sijmons RH, Leegte B, van Lingen RA, de Pater JM, van der Veen AY, del Canho H, Bos C, ten Kate LP, Breed AS. Sijmons RH, et al. Am J Med Genet. 1993 Sep 15;47(4):559-62. doi: 10.1002/ajmg.1320470424. Am J Med Genet. 1993. PMID: 7504882

6

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. Am J Med Genet. 1999 Sep 10;86(2):168-73. doi: 10.1002/(sici)1096-8628(19990910)86:2<168::aid-ajmg16>3.0.co;2-q. Am J Med Genet. 1999. PMID: 10449655 Review.

7

Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.

Tan-Sindhunata G, Castedo S, Leegte B, Mulder I, vd Veen AY, vd Hout AH, Wiersma TJ, van Essen AJ. Tan-Sindhunata G, et al. Am J Med Genet. 2000 May 15;92(2):147-52. Am J Med Genet. 2000. PMID: 10797441

8

11q- syndrome: three cases and a review of the literature.

Leegte B, Kerstjens-Frederikse WS, Deelstra K, Begeer JH, van Essen AJ. Leegte B, et al. Genet Couns. 1999;10(3):305-13. Genet Couns. 1999. PMID: 10546104 Review.

9

Phenotypic variability of Cat-Eye syndrome.

Berends MJ, Tan-Sindhunata G, Leegte B, van Essen AJ. Berends MJ, et al. Genet Couns. 2001;12(1):23-34. Genet Couns. 2001. PMID: 11332976 Review.

10

Trisomy 1q42 --> qter in a sister and brother: further delineation of the "trisomy 1q42 --> qter syndrome".

Verschuuren-Bemelmans CC, Leegte B, Hodenius TM, Cobben JM. Verschuuren-Bemelmans CC, et al. Am J Med Genet. 1995 Jul 31;58(1):83-6. doi: 10.1002/ajmg.1320580116. Am J Med Genet. 1995. PMID: 7573162 Review.

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