Authors:
Verhoog, LC
van den Ouweland, AMW
Berns, E
van Veghel-Plandsoen, MM
van Staveren, IL
Wagner, A
Bartels, CCM
Tilanus-Linthorst, MMA
Devilee, P
Seynaeve, C
Halley, DJJ
Niermeijer, MF
Klijn, JGM
Meijers-Heijboer, H
Citation: Lc. Verhoog et al., Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families, EUR J CANC, 37(16), 2001, pp. 2082-2090
Authors:
Meijers-Heijboer, H
van Geel, B
van Putten, WLJ
Henzen-Logmans, SC
Seynaeve, C
Menke-Pluymers, MBE
Bartels, CCM
Verhoog, LC
van den Ouweland, AMW
Niermeijer, MF
Brekelmans, CTM
Klijn, JGM
Citation: H. Meijers-heijboer et al., Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation., N ENG J MED, 345(3), 2001, pp. 159-164
Authors:
Berns, EMJJ
van Staveren, IL
Verhoog, L
van de Ouweland, AMW
Meijer-van Gelder, M
Meijers-Heijboer, H
Portengen, H
Foekens, JA
Dorssers, LCJ
Klijn, JGM
Citation: Emjj. Berns et al., Molecular profiles of BRCA1-mutated and matched sporadic breast tumours: relation with clinico-pathological features, BR J CANC, 85(4), 2001, pp. 538-545
Authors:
de Leeuw, WJF
Dierssen, J
Vasen, HFA
Wijnen, JT
Kenter, GG
Meijers-Heijboer, H
Brocker-Vriends, A
Stormorken, A
Moller, P
Menko, F
Cornelisse, CJ
Morreau, H
Citation: Wjf. De Leeuw et al., Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients, J PATHOLOGY, 192(3), 2000, pp. 328-335
Authors:
Meijers-Heijboer, H
Lindhout, D
Menko, F
Vossen, S
Moslein, G
Tops, C
Brocker-Vriends, A
Wu, Y
Hofstra, R
Sijmons, R
Cornelisse, C
Morreau, H
Fodde, R
Citation: H. Meijers-heijboer et al., Familial endometrial cancer in female carriers of MSH6 germline mutations, NAT GENET, 23(2), 1999, pp. 142-144
Authors:
Fang, P
Lev-Lehman, E
Tsai, TF
Matsuura, T
Benton, CS
Sutcliffe, JS
Christian, SL
Kubota, T
Halley, DJ
Meijers-Heijboer, H
Langlois, S
Graham, JM
Beuten, J
Willems, PJ
Ledbetter, DH
Beaudet, AL
Citation: P. Fang et al., The spectrum of mutations in UBE3A causing Angelman syndrome, HUM MOL GEN, 8(1), 1999, pp. 129-135