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au.\*:("VERHOEF, S")

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Cancer risks in BRCA2 families : estimates for sites other than breast and ovaryVAN ASPEREN, C. J; BROHET, R. M; HOGERVORST, F. B. L et al.Journal of medical genetics. 2005, Vol 42, Num 9, pp 711-719, issn 0022-2593, 9 p.Article

High rate of mosaicism in tuberous sclerosis complexVERHOEF, S; BAKKER, L; LINDHOUT, D et al.American journal of human genetics. 1999, Vol 64, Num 6, pp 1632-1637, issn 0002-9297Article

Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis familiesJANSSEN, B; SAMPSON, J; SANDKUIJL, L et al.Human genetics. 1994, Vol 94, Num 4, pp 437-440, issn 0340-6717Article

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2OSORIO, A; MILNE, R. L; KONSTANTOPOULOU, I et al.British journal of cancer. 2011, Vol 104, Num 8, pp 1356-1361, issn 0007-0920, 6 p.Article

A multiplex PCR predictor for aCGH success of FFPE samplesVAN BEERS, E. H; JOOSSE, S. A; LIGTENBERG, M. J et al.British journal of cancer. 2006, Vol 94, Num 2, pp 333-337, issn 0007-0920, 5 p.Article

Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large familyVERHOEF, S; SCHRANDER-STUMPEL, C. T. R. M; VUZEVSKI, V. D et al.Journal of medical genetics. 1998, Vol 35, Num 10, pp 841-845, issn 0022-2593Article

Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexVRTEL, R; VERHOEF, S; HOFF, M et al.Journal of medical genetics. 1996, Vol 33, Num 1, pp 47-51, issn 0022-2593Article

Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distressLAMMENS, Crm; BLEIKER, Ema; HOOGERBRUGGE, N et al.Clinical genetics. 2010, Vol 77, Num 5, pp 483-491, issn 0009-9163, 9 p.Article

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA I and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCAI/BRCA2 (CIMBA)OSORIO, A; MILNE, R. L; HEALEY, S et al.British journal of cancer. 2009, Vol 101, Num 12, pp 2048-2054, issn 0007-0920, 7 p.Article

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of itoEUSSEN, B. H. J; BARTALINI, G; HALLEY, D. J. J et al.Journal of medical genetics. 2000, Vol 37, Num 4, pp 287-291, issn 0022-2593Article

Uniparental disomy with and without confined placental mosaicism : A model for trisomic zygote rescueLOS, F. J; VAN OPSTAL, D; VAN DEN BERG, C et al.Prenatal diagnosis. 1998, Vol 18, Num 7, pp 659-668, issn 0197-3851Article

The evolution of renal angiomyolipomas in patients with tuberous sclerosisVAN BAAL, J. G; SMITS, N. J; KEEMAN, J. N et al.The Journal of urology. 1994, Vol 152, Num 1, pp 35-38, issn 0022-5347Article

Validating measures of free-living physical activity in overweight and obese subjects using an accelerometerVALENTI, G; CAMPS, S. G. J. A; VERHOEF, S. P. M et al.International journal of obesity. 2014, Vol 38, Num 7, pp 1011-1014, issn 0307-0565, 4 p.Article

The relationship between leptin, gonadotropic hormones, and body composition during puberty in a Dutch children cohortRUTTERS, F; NIEUWENHUIZEN, A. G; VERHOEF, S. P. M et al.European journal of endocrinology. 2009, Vol 160, Num 6, pp 973-978, issn 0804-4643, 6 p.Article

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