Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age von van der Kolk, Dorina M, de Bock, Geertruida H, Leegte, Beike K, Schaapveld, Michael, Mourits, Marian J. E, de Vries, Jakob, van der Hout, Annemieke H, Oosterwijk, Jan C

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Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co‐occurring FANCC and CHEK2 mutations von Berger, Gerbrig, Berg, Eva, Smetsers, Stephanie, Leegte, Beike K., Sijmons, Rolf H., Abbott, Kristin M., Mulder, André B., Vellenga, Edo

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Time to stop ovarian cancer screening in BRCA1/2 mutation carriers? von van der Velde, Nienke M., Mourits, Marian J.E., Arts, Henriëtte J.G., de Vries, Jacob, Leegte, Beike K., Dijkhuis, Grieteke, Oosterwijk, Jan C., de Bock, Geertruida H.

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Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in and families: high cancer incidence at older age von Kolk, Dorina M., Bock, Geertruida H., Leegte, Beike K., Schaapveld, Michael, Mourits, Marian J. E., Vries, Jakob, Hout, Annemieke H., Oosterwijk, Jan C.

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Practical guidelines for interpreting copy number gains detected by high-resolution array CGH in routine diagnostics von van Ravenswaaij-Arts, Conny M.A., Sikkema-Raddatz, Birgit, van Der Vries, Gerben, Dijkhuizen, Trijnie, Hanemaaijer, Nicolien M., Hordijk, Roel, van Essen, Ton J., Veenstra-Knol, Irma (h.) E., Kerstjens-Frederikse, W S, Herkert, J C, Gerkes, Erica, Leegte, Beike (l.) K., Kok, Klaas, Sinke, Richard J.

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Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype von Hordijk, Roel, Wierenga, Henk, Scheffer, Hans, Leegte, Beike, Hofstra, Robert M W, Stolte-Dijkstra, Irene

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Two unbalanced segregation products due to a maternal t(7;16)inv(16) von Leegte, Beike, Sikkema-Raddatz, Birgit, Hordijk, Roel, Davelaar, Inge, van der Veen, Anneke, Cobben, JanMaarten

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Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22 von Verheij, Joke B.G.M., Bouman, Katelÿne, van Lingen, Richard A., van Lookeren Campagne, Joannes G., Leegte, Beike, van der Veen, Anneke Y., Hofstra, Robert M.W., Buys, Charles H.C.M., van Essen, Anthonie J.

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Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype von Tan-Sindhunata, Gita, Castedo, Sérgio, Leegte, Beike, Mulder, Irma, vd Veen, Anneke Y., vd Hout, Annemieke H., Wiersma, Titte J., Van Essen, Anthonie J.

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Three cases of mosaicism for balanced reciprocal translocations von Leegte, Beike, Sikkema-Raddatz, Birgit, Hordijk, Roel, Bouman, Katelijne, van Essen, Ton, Castedo, Sergio, de Jong, Bauke

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Cytogenetic evidence that carcinoma in situ is the precursor lesion for invasive testicular germ cell tumors von van Echten, Jannie, Stoepker, Marian, Leegte, Beike, Looijenga, Leendert, de Jong, Bauke, Wolter Oosterhuis, J

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Trisomy 1q42→qter in a sister and brother: Further delineation of the "trisomy 1q42→qter Syndrome" von Verschuuren-Bemelmans, Corien C., Leegte, Beike, Hodenius, Thea M. J., Cobben, Jan M.

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Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)] von Sijmons, Rolf H., Leegte, Beike, Van Lingen, Richard A., De Pater, Joke M., Van Der Veen, Anneke Y., Canho, Harrij Del, Bos, Carla, Kate, Leo P. Ten, Breed, Anton S. P. M.

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