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Author/Creator Hogervorst, Frans B L

1. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations. Issue 2 (27th November 2013)

Authors:
Brohet, Richard M; Velthuizen, Maria E; Hogervorst, Frans B L; EJ Meijers-Heijboer, Hanne; Seynaeve, Caroline; Collée, Margriet J; Verhoef, Senno; Ausems, Margreet G E M; Hoogerbrugge, Nicoline; van Asperen, Christi J; Gómez García, Encarna; Menko, Fred; Oosterwijk, Jan C; Devilee, Peter; Veer, L...
Other Names:
Rookus MA author non-byline.; Brohet RM author non-byline.; Hogervorst FBL author non-byline.; van Leeuwen FE author non-byline.; Verhoef S author non-byline.; Schmidt MK author non-byline.; de Lange JL author non-byline.; Collée JM author non-byline.; van den Ouweland AMW author non-byline.; Hoo...
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 2(2014)
Page Start:
98
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. Issue 12 (5th November 2011)

Authors:
Adank, Muriel A; Jonker, Marianne A; Kluijt, Irma; van Mil, Saskia E; Oldenburg, Rogier A; Mooi, Wolter J; Hogervorst, Frans B L; van den Ouweland, Ans M W; Gille, Johan J P; Schmidt, Marjanka K; van der Vaart, Aad W; Meijers-Heijboer, Hanne; Waisfisz, Quinten
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 12(2011)
Page Start:
860
Record Type:
Journal Article
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3. TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes. Issue 6 (3rd June 2010)

Authors:
Ruijs, Marielle W G; Verhoef, Senno; Rookus, Matti A; Pruntel, Roelof; van der Hout, Annemarie H; Hogervorst, Frans B L; Kluijt, I; Sijmons, Rolf H; Aalfs, Cora M; Wagner, Anja; Ausems, Margreet G E M; Hoogerbrugge, Nicoline; van Asperen, Christi J; Gomez Garcia, Encarna B; Meijers-Heijboer, Hann...
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 6(2010)
Page Start:
421
Record Type:
Journal Article
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4. Variants of Uncertain Significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counselling. Issue 2 (11th December 2012)

Authors:
Moghadasi, Setareh; Hofland, Nandy; Wouts, Joyce N; Hogervorst, Frans B L; Wijnen, Juul T; Vreeswijk, Maaike P G; van Asperen, Christi J
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 2(2013)
Page Start:
74
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗