Berends MJ - Search Results

1

Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype.

Berends MJ, Hordijk R, Scheffer H, Oosterwijk JC, Halley DJ, Sorgedrager N. Berends MJ, et al. Am J Med Genet. 1999 May 7;84(1):76-9. doi: 10.1002/(sici)1096-8628(19990507)84:1<76::aid-ajmg16>3.0.co;2-f. Am J Med Genet. 1999. PMID: 10213052 No abstract available.

2

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

Wu Y, Berends MJ, Mensink RG, Kempinga C, Sijmons RH, van Der Zee AG, Hollema H, Kleibeuker JH, Buys CH, Hofstra RM. Wu Y, et al. Among authors: berends mj. Am J Hum Genet. 1999 Nov;65(5):1291-8. doi: 10.1086/302612. Am J Hum Genet. 1999. PMID: 10521294 Free PMC article.

3

The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

Landsvater RM, Rombouts AG, te Meerman GJ, Schillhorn-van Veen JM, Berends MJ, Geerdink RA, Struyvenberg A, Buys CH, Lips CJ. Landsvater RM, et al. Among authors: berends mj. Am J Hum Genet. 1993 Feb;52(2):335-42. Am J Hum Genet. 1993. PMID: 8094268 Free PMC article.

4

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant.

Berends MJ, Wu Y, Sijmons RH, Mensink RG, van der Sluis T, Hordijk-Hos JM, de Vries EG, Hollema H, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, Kleibeuker JH. Berends MJ, et al. Am J Hum Genet. 2002 Jan;70(1):26-37. doi: 10.1086/337944. Am J Hum Genet. 2002. PMID: 11709755 Free PMC article.

5

Colorectal cancer and the CHEK2 1100delC mutation.

de Jong MM, Nolte IM, Te Meerman GJ, van der Graaf WT, Mulder MJ, van der Steege G, Bruinenberg M, Schaapveld M, Niessen RC, Berends MJ, Sijmons RH, Hofstra RM, de Vries EG, Kleibeuker JH. de Jong MM, et al. Among authors: berends mj. Genes Chromosomes Cancer. 2005 Aug;43(4):377-82. doi: 10.1002/gcc.20195. Genes Chromosomes Cancer. 2005. PMID: 15852425

6

No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk.

de Jong MM, Hofstra RM, Kooi KA, Westra JL, Berends MJ, Wu Y, Hollema H, van der Sluis T, van der Graaf WT, de Vries EG, Schaapveld M, Sijmons RH, te Meerman GJ, Kleibeuker JH. de Jong MM, et al. Among authors: berends mj. Cancer Genet Cytogenet. 2004 Jul 1;152(1):70-1. doi: 10.1016/j.cancergencyto.2003.10.008. Cancer Genet Cytogenet. 2004. PMID: 15193445

7

Long-term follow-up in four large MEN 2 families in The Netherlands.

Lips CJ, Berends MJ, Brouwers-Smalbraak J, Geerdink RA, Hackeng WH, Jansen-Schillhorn van Veen JM, Struyvenberg A, van Vroonhoven TJ. Lips CJ, et al. Among authors: berends mj. Henry Ford Hosp Med J. 1992;40(3-4):256-7. Henry Ford Hosp Med J. 1992. PMID: 1362417

8

A role for MLH3 in hereditary nonpolyposis colorectal cancer.

Wu Y, Berends MJ, Sijmons RH, Mensink RG, Verlind E, Kooi KA, van der Sluis T, Kempinga C, van dDer Zee AG, Hollema H, Buys CH, Kleibeuker JH, Hofstra RM. Wu Y, et al. Among authors: berends mj. Nat Genet. 2001 Oct;29(2):137-8. doi: 10.1038/ng1001-137. Nat Genet. 2001. PMID: 11586295

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

Thyroid C-cell hyperplasia and micronodules in close relatives of MEN-2A patients: pitfalls in early diagnosis and reevaluation of criteria for surgery.

Lips CJ, Leo JR, Berends MJ, Minder WH, Blok AP, Geerdink RA, Hackeng WH, Roelofs JM, Vasen HF, Vette JK. Lips CJ, et al. Among authors: berends mj. Henry Ford Hosp Med J. 1987;35(2-3):133-8. Henry Ford Hosp Med J. 1987. PMID: 2891645 No abstract available.

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