Gille JJ - Search Results

1

Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.

Menko FH, Kneepkens CM, de Leeuw N, Peeters EA, Van Maldergem L, Kamsteeg EJ, Davidson R, Rozendaal L, Lasham CA, Peeters-Scholte CM, Jansweijer MC, Hilhorst-Hofstee Y, Gille JJ, Heins YM, Nieuwint AW, Sistermans EA. Menko FH, et al. Among authors: gille jj. Clin Genet. 2008 Aug;74(2):145-54. doi: 10.1111/j.1399-0004.2008.01026.x. Epub 2008 May 28. Clin Genet. 2008. PMID: 18510548 Free article.

2

Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literature.

de Ru MH, Gille JJ, Nieuwint AW, Bijlsma JB, van der Blij JF, van Hagen JM. de Ru MH, et al. Among authors: gille jj. Am J Med Genet A. 2005 Aug 15;137(1):81-7. doi: 10.1002/ajmg.a.30786. Am J Med Genet A. 2005. PMID: 16015581 Review.

3

A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer.

Menko FH, Kaspers GL, Meijer GA, Claes K, van Hagen JM, Gille JJ. Menko FH, et al. Among authors: gille jj. Fam Cancer. 2004;3(2):123-7. doi: 10.1023/B:FAME.0000039893.19289.18. Fam Cancer. 2004. PMID: 15340263

4

Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.

Nahorski MS, Lim DH, Martin L, Gille JJ, McKay K, Rehal PK, Ploeger HM, van Steensel M, Tomlinson IP, Latif F, Menko FH, Maher ER. Nahorski MS, et al. Among authors: gille jj. J Med Genet. 2010 Jun;47(6):385-90. doi: 10.1136/jmg.2009.073304. J Med Genet. 2010. PMID: 20522427

5

STRAD in Peutz-Jeghers syndrome and sporadic cancers.

de Leng WW, Keller JJ, Luiten S, Musler AR, Jansen M, Baas AF, de Rooij FW, Gille JJ, Menko FH, Offerhaus GJ, Weterman MA. de Leng WW, et al. Among authors: gille jj. J Clin Pathol. 2005 Oct;58(10):1091-5. doi: 10.1136/jcp.2005.026013. J Clin Pathol. 2005. PMID: 16189157 Free PMC article.

6

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach.

Gille JJ, Hogervorst FB, Pals G, Wijnen JT, van Schooten RJ, Dommering CJ, Meijer GA, Craanen ME, Nederlof PM, de Jong D, McElgunn CJ, Schouten JP, Menko FH. Gille JJ, et al. Br J Cancer. 2002 Oct 7;87(8):892-7. doi: 10.1038/sj.bjc.6600565. Br J Cancer. 2002. PMID: 12373605 Free PMC article.

7

Clinical and genetic evaluation of thirty ovarian cancer families.

Zweemer RP, Verheijen RH, Gille JJ, van Diest PJ, Pals G, Menko FH. Zweemer RP, et al. Among authors: gille jj. Am J Obstet Gynecol. 1998 Jan;178(1 Pt 1):85-90. doi: 10.1016/s0002-9378(98)70632-5. Am J Obstet Gynecol. 1998. PMID: 9465809

8

Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data.

van der Groep P, Bouter A, van der Zanden R, Siccama I, Menko FH, Gille JJ, van Kalken C, van der Wall E, Verheijen RH, van Diest PJ. van der Groep P, et al. Among authors: gille jj. J Clin Pathol. 2006 Jun;59(6):611-7. doi: 10.1136/jcp.2005.032151. Epub 2006 Apr 7. J Clin Pathol. 2006. PMID: 16603649 Free PMC article.

9

A case of loss of heterozygosity in the BRCA2 gene of a borderline ovarian tumor: case report and review of literature.

Verbruggen MB, Zweemer RP, Piek JM, van Unnik GA, van Diest PJ, Gille JJ, Menko FH, Dorsman JC, Verheijen RH. Verbruggen MB, et al. Among authors: gille jj. Int J Gynecol Cancer. 2007 Sep-Oct;17(5):1143-7. doi: 10.1111/j.1525-1438.2007.00924.x. Epub 2007 Mar 26. Int J Gynecol Cancer. 2007. PMID: 17386038 Review.

10

[Patient with Peutz-Jeghers syndrome and liver metastases from an unknown primary tumor].

van der Werf G, Menko FH, Gille JJ, van Diest PJ, van Groeningen CJ. van der Werf G, et al. Among authors: gille jj. Ned Tijdschr Geneeskd. 2000 Apr 1;144(14):667-70. Ned Tijdschr Geneeskd. 2000. PMID: 10774296 Review. Dutch.

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