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  11. An amendment to this paper has been published and can be accessed via the original article.

    Authors: Zelmira Ballatore, Raffaella Bracci, Elena Maccaroni, Lucia Svarca, Francesca Bianchi, Laura Belvederesi, Cristiana Brugiati, Silvia Pagliaretta, Alberto Murrone, Federica Bini, Mirco Pistelli, Giulia Ricci and Rossana Berardi
    Citation: Hereditary Cancer in Clinical Practice 2020 18:11
    Content type: Correction Published on:

    The original article was published in Hereditary Cancer in Clinical Practice 2020 18:10

  16. Authors: Katarzyna Kaczmarek, Anna Jakubowska, Grzegorz Sukiennicki, Magdalena Muszyńska, Katarzyna Jaworska-Bieniek, Katarzyna Durda, Tomasz Huzarski, Pablo Serrano-Fernandez, Tomasz Byrski, Jacek Gronwald, Satish Gupta and Jan Lubiński
    Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 4):A6
    Content type: Meeting abstract Published on:

    This article is part of a Supplement: Volume 10 Supplement 4

  17. Authors: Katarzyna Kaczmarek, Magdalena Muszyńska, Katarzyna Jaworska-Bieniek, Wojciech Marciniak, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Tomasz Gromowski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska…
    Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A4
    Content type: Meeting abstract Published on:

    This article is part of a Supplement: Volume 13 Supplement 2

  27. Authors: Wojciech Marciniak, Magdalena Muszyńska, Katarzyna Jaworska-Bieniek, Katarzyna Kaczmarek, Grzegorz Sukiennicki, Marcin Lener, Katarzyna Durda, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Oleg Oszurek, Cezary Cybulski, Tadeusz Dębniak, Antoni Morawski, Anna Jakubowska and Jan Lubiński
    Citation: Hereditary Cancer in Clinical Practice 2015 13(Suppl 2):A6
    Content type: Meeting abstract Published on:

    This article is part of a Supplement: Volume 13 Supplement 2

  32. Authors: Georgia Chenevix-Trench, Yi Lu, Sharon Johnatty, Eric Gamazon, Jonathan Beesley, Xiaoqing Chen, Bo Gao, Paul Harnett, R Stephanie Huang, Evelyn Despierre, Florian Heitz, Estrid Hogdall, Claus Hogdall, Robert Brown, Kirsten Moyisch, Peter Fasching…
    Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A36
    Content type: Meeting abstract Published on:

    This article is part of a Supplement: Volume 10 Supplement 2

  33. Authors: MC Southey, DJ Park, F Lesueur, F Odefrey, T Nguyen-Dumont, F Hammet, SL Neuhausen, EM John, IL Andrulis, G Chenevix-Trench, L Baglietto, F Le Calvez-Kelm, M Pertesi, A Lonie, B Pope, O Sinilnikova…
    Citation: Hereditary Cancer in Clinical Practice 2012 10(Suppl 2):A40
    Content type: Meeting abstract Published on:

    This article is part of a Supplement: Volume 10 Supplement 2

  35. Authors: Aung K Win, Sean P Cleary, James G Dowty, Noralane M Lindor, Polly A Newcomb, Robert W Haile, Joanne P Young, Daniel D Buchanan, Loïc Le Marchand, Roger Green, John L Hopper, Steven Gallinger and Mark A Jenkins
    Citation: Hereditary Cancer in Clinical Practice 2011 9(Suppl 1):P40
    Content type: Poster presentation Published on:

    This article is part of a Supplement: Volume 9 Supplement 1

  38. A consanguineous family of three siblings presented with different early onset pediatric cancers. Whole-exome sequencing of parents DNA revealed a deleterious frameshift mutation in hPMS1 the first to be reported...

    Authors: Reem S. Hamad and Muntaser E. Ibrahim
    Citation: Hereditary Cancer in Clinical Practice 2022 20:16
    Content type: Letter to the Editor Published on:

  42. PIK3CA is the most frequently mutated oncogene in human cancers. PIK3CA is phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha. It controls cell growth, proliferation, motility, survival, d...

    Authors: Sidra German, Hafiz Muhammad Aslam, Shafaq Saleem, Aisha Raees, Tooba Anum, Arsalan Ahmad Alvi and Abdul Haseeb
    Citation: Hereditary Cancer in Clinical Practice 2013 11:5
    Content type: Letter to the Editor Published on:

  44. A family is reported in which three male siblings of Asian descent developed non-Hodgkin's lymphoma (NHL). Case 1 was diagnosed with indolent follicular lymphoma stage IIIA at age 45. Case 2 presented with lar...

    Authors: Sandra S.C.M. Loves, Lieuwe de Haan and Simon M.G.J. Daenen
    Citation: Hereditary Cancer in Clinical Practice 2006 4:136
    Content type: Case report Published on:

  47. The editors of Hereditary Cancer in Clinical Practice would like to thank all our reviewers who have contributed to the journal in 2014.

    Authors: Jan Lubinski, Rodney J Scott, Rolf Sijmons and Katie Bayliss
    Citation: Hereditary Cancer in Clinical Practice 2015 13:9
    Content type: Reviewer acknowledgement Published on:
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Hereditary Cancer in Clinical Practice

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