Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma

    Brandal, P., Panagopoulos, I., Bjerkehagen, B. & Heim, S., 2009, I : Genes, Chromosomes and Cancer. 48, 12, s. 1051-1056

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. Proliferative activity and number of clonal chromosome aberrations in non‐Hodgkin's lymphomas

    Brandt, L., Ulf Kristoffersson & Håkan Olsson, 1986 jan 1, I : Scandinavian Journal of Haematology. 37, 2, s. 106-110

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer

    O Bratt, Damber, J. E., Emanuelsson, M., U Kristoffersson, Lundgren, R., Håkan Olsson & Grönberg, H., 2000 jan, I : European Journal of Cancer. 36, 2, s. 235-241

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study

    O Bratt, U Kristoffersson, Lundgren, R. & Håkan Olsson, 1999 feb, I : European Journal of Cancer. 35, 2, s. 272-7 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor

    O Bratt, U Kristoffersson, Håkan Olsson & Lundgren, R., 1998, I : European Urology. 34, 1, s. 19-24 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Forskningsframsteg om hereditär prostatacancer. Riskfamiljer bör kartläggas och erbjudas screening

    O Bratt, Abrahamsson, P. A., Lundgren, R., Håkan Olsson & U Kristoffersson, 1998 apr 1, I : Läkartidningen. 95, 14, s. 1494-6 3 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Sons of men with prostate cancer: their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing

    O Bratt, U Kristoffersson, Lundgren, R. & Håkan Olsson, 1997 sep, I : Urology. 50, 3, s. 360-5 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

    Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., de Pauw, A., Tischkowitz, M., Hans Ehrencrona, Dolbeault, S., Robieux, L., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D. & Schmutlzer, R., 2018, I : Familial Cancer. 17, 1, s. 31-41

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey

    Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., de Pauw, A., Tischkowitz, M., Hans Ehrencrona, Schmidt, M. K., Dolbeault, S., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D. & Schmutlzer, R., 2019 jan, I : Journal of Community Genetics. 10, 1, s. 61-71

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors

    Brekke, H. R., Kolberg, M., Skotheim, R. I., Hall, K. S., Bjerkehagen, B., Risberg, B., Domanski, H., Nils Mandahl, Liestol, K., Smeland, S., Danielsen, H. E., Fredrik Mertens & Lothe, R. A., 2009, I : Neuro-Oncology. 11, 5, s. 514-528

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.

    Brekke, H. R., Ribeiro, F. R., Kolberg, M., Agesen, T. H., Lind, G. E., Eknæs, M., Hall, K. S., Bjerkehagen, B., van den Berg, E., Teixeira, M. R., Nils Mandahl, Smeland, S., Fredrik Mertens, Skotheim, R. I. & Lothe, R. A., 2010, I : Journal of Clinical Oncology. 28, s. 1573-1582

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia

    Broberg, K., Sören Toksvig-Larsen, Lindstrand, A. & Fredrik Mertens, 2001, I : Genes, Chromosomes and Cancer. 30, 3, s. 310-315

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. Characterization of somatic mutations in nonneoplastic cells

    Broberg, K., 2001, Department of Clinical Genetics, Lund University. 110 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  14. Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis

    K Broberg, M Höglund, Limon, J., Lindstrand, A., S Toksvig-Larsen, N Mandahl & F Mertens, 1999 mar, I : Genes, Chromosomes and Cancer. 24, 3, s. 278-82

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis

    Broberg, K., Limon, J., Pålsson, E., Lindstrand, A., S Toksvig-Larsen, N Mandahl & F Mertens, 1997 dec, I : Human Genetics. 101, 3, s. 295-8 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.

    Karin Broberg Palmgren, Jonas Björk, Paulsson, K., Mattias Höglund & Maria Albin, 2005, I : Carcinogenesis. 26, 7, s. 1263-1271

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia

    Karin Broberg Palmgren, Tallini, G., Mattias Höglund, Lindstrand, A., Sören Toksvig-Larsen & Fredrik Mertens, 2001, I : Modern Pathology. 14, 4, s. 311-317

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.

    Karin Broberg Palmgren, Zhang, M., Strömbeck, B., Isaksson, M., Nilsson, M. A., Fredrik Mertens, Nils Mandahl & Panagopoulos, I., 2002, I : International Journal of Oncology. 21, 2, s. 321-326

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes

    Broliden, PA., Dahl, IM., Hast, R., Bertil Johansson, Juvonen, E., Kjeldsen, L., Porwit-MacDonald, A., Sjoo, M., Tangen, JM., Uggla, B., Oberg, G. & Hellstrom-Lindberg, E., 2006, I : Haematologica. 91, 5, s. 667-670

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells

    Brun, A., Björnsson, J. M., Mattias Magnusson, Larsson, N., Levéen, P., Mats Ehinger, Nilsson, E. C. & Stefan Karlsson, 2004, I : Blood. 103, 11, s. 4126-4133

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  21. Mesenchymal stromal cells from primary osteosarcoma are non-malignant and strikingly similar to their bone marrow counterparts.

    Brune, J. C., Tormin, A., Maria C Johansson, Rissler, P., Brosjö, O., Löfvenberg, R., Fredrik Vult von Steyern, Fredrik Mertens, Anders Rydholm & Stefan Scheding, 2011, I : International Journal of Cancer. 129, s. 319-330

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.

    Buckley, P. G., Mantripragada, K. K., Benetkiewicz, M., Tapia-Páez, I., Diaz De Ståhl, T., Rosenquist, M., Ali, H., Jarbo, C., De Bustos, C., Hirvelä, C., Sinder Wilén, B., Fransson, I., Thyr, C., Johnsson, B-I., Bruder, C. E. G., Menzel, U., Hergersberg, M., Mandahl, N., Blennow, E., Wedell, A. & 11 andraBeare, D. M., Collins, J. E., Dunham, I., Albertson, D., Pinkel, D., Bastian, B. C., Faruqi, A. F., Lasken, R. S., Ichimura, K., Collins, V. P. & Dumanski, J. P., 2002, I : Human Molecular Genetics. 11, 25, s. 3221-3229

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R. A. J., Buerger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoom, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, I : Clinical Cancer Research. 17, 8, s. 2110-2119

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage-Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R., Burger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoorn, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, I : Laboratory Investigation. 91, Feb 26 - Mar 4, 2011, s. 10A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  25. Tumors of endocrine glands

    Bullerdiek, J. & David Gisselsson, 2015, Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells. Heim, S. & Mitelman, F. (red.). 4th uppl. Wiley-Blackwell, s. 497-514 18 s.

    Forskningsoutput: Kapitel i bok/rapport/Conference proceedingKapitel samlingsverk

  26. Generation of human cortical neurons from a new immortal fetal neural stem cell line.

    Cacci, E., Villa, A., Malin Parmar, Cavallaro, M., Nils Mandahl, Olle Lindvall, Martinez-Serrano, A. & Zaal Kokaia, 2007, I : Experimental Cell Research. 313, 3, s. 588-601

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. Telomere dysfunction and telomerase activation in cancer - a pathological paradox?

    Calcagnile, O. & David Gisselsson Nord, 2007, I : Cytogenetic and Genome Research. 118, 2-4, s. 270-276

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

    Calefato, J-M., Nippert, I., Harris, H. J., Ulf Kristoffersson, Schmidtke, J., Ten Kate, L. P., Anionwu, E., Benjamin, C., Challen, K., Plass, A-M., Harris, R. & Julian-Reynier, C., 2008, I : Genetics in Medicine. 10, 2, s. 99-106

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia

    Callen, D. F., Hull, Y. J., Toogood, I. R., Thoas Fioretos, Heim, S., Nils Mandahl & Felix Mitelman, 1991, I : Cancer Genetics and Cytogenetics. 51, 2, s. 255-258

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. Unaltered pancreatic islet blood perfusion in islet amyloid polypeptide-deficient mice

    Carlsson, PO., Karlsson, E., Hindrik Mulder & Samuel Gebre-Medhin, 2002, I : European Journal of Endocrinology. 146, 1, s. 107-112

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  31. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

    Carpten, JD., Robbins, CM., Villablanca, A., Forsberg, L., Presciuttini, S., Bailey-Wilson, J., Simonds, WF., Gillanders, EM., Kennedy, AM., Chen, JD., Agarwal, SK., Sood, R., Jones, MP., Moses, TY., Haven, C., Petillo, D., Leotlela, PD., Harding, B., Cameron, D., Pannett, AA. & 21 andraHoog, A., Heath, H., James-Newton, LA., Robinson, B., Zarbo, RJ., Cavaco, BM., Wassif, W., Perrier, ND., Rosen, IB., Ulf Kristoffersson, Turnpenny, PD., Farnebo, LO., Besser, GM., Jackson, CE., Morreau, H., Trent, JM., Thakker, RV., Marx, SJ., Teh, BT., Larsson, C. & Hobbs, MR., 2002, I : Nature Genetics. 32, 4, s. 676-680

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

    Castellani, C., Macek, M. J., Cassiman, J-J., Duff, A., Massie, J., ten Kate, L. P., Barton, D., Cutting, G., Dallapiccola, B., Dequeker, E., Girodon, E., Grody, W., Highsmith, E. W., Kaariainen, H., Kruip, S., Morris, M., Pignatti, P. F., Pypops, U., Schwarz, M., Soller, M. & 2 andraStuhrman, M. & Cuppens, H., 2010, I : Journal of Cystic Fibrosis. 9, 3, s. 165-178

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  33. Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.

    Anders Castor, Nilsson, L., Åstrand-Grundström, I., Buitenhuis, M., Ramirez, C., Anderson, K., Strömbeck, B., Garwicz, S., Békássy, A., Schmiegelow, K., Lausen, B., Hokland, P., Lehmann, S., Gunnar Juliusson, Bertil Johansson & Jacobsen, S. E. W., 2005, I : Nature Medicine. 11, 6, s. 630-637

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  34. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

    Catucci, I., Osorio, A., Arver, B., Neidhardt, G., Bogliolo, M., Zanardi, F., Riboni, M., Minardi, S., Pujol, R., Azzollini, J., Peissel, B., Manoukian, S., De Vecchi, G., Casola, S., Hauke, J., Richters, L., Rhiem, K., Schmutzler, R. K., Wallander, K., Törngren, T. & 8 andraÅke Borg, Radice, P., Surrallés, J., Hahnen, E., Hans Ehrencrona, Anders Kvist, Benitez, J. & Peterlongo, P., 2018, I : Genetics in Medicine. 20, s. 452–457 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. Gain of 1q as a prognostic biomarker in Wilms Tumors (WTs) treated with preoperative chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 trial: A SIOP renal tumours biology consortium study

    Chagtai, T., Zill, C., Dainese, L., Wegert, J., Savola, S., Popov, S., Mifsud, W., Vujanić, G., Sebire, N., Le Bouc, Y., Ambros, P. F., Kager, L., O'Sullivan, M. J., Blaise, A., Bergeron, C., Mengelbier, L. H., Gisselsson, D., Kool, M., Tytgat, G. A. M., Van Den Heuvel-Eibrink, M. M. & 6 andraGraf, N., Van Tinteren, H., Coulomb, A., Gessler, M., Williams, R. D. & Pritchard-Jones, K., 2016 sep 10, I : Journal of Clinical Oncology. 34, 26, s. 3195-3203 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.

    Challen, K., Harris, H., Julian-Reynier, C., Ten Kate, L., Ulf Kristoffersson, Nippert, I., Schmidtke, J., Benjamin, C. & Harris, R., 2005, I : Genetics in Medicine. 7, 5, s. 302-310

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  37. Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort

    U. Chaudhry, P. G. Platonov, Rubulis, A., Bergfeldt, L., Jensen, S. M., Lundin, C. & R. Borgquist, 2019, I : Journal of Electrocardiology. 56, s. 46-51 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  38. Better Prognosis of Patients with Glioma Expressing FGF2-Dependent PDGFRA Irrespective of Morphological Diagnosis.

    Chen, D., Persson, A., Sun, Y., Leif Salford, David Gisselsson Nord, Elisabet Englund, Jiang, T. & Xiaolong Fan, 2013, I : PLoS ONE. 8, 4, e61556.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. L1 syndrome diagnosis complemented with functional analysis of L1CAM variants located to the two N-terminal Ig-like domains.

    Christaller, W. A. A., Vos, Y., Samuel Gebre-Medhin, Hofstra, R. M. W. & Schäfer, M. K. E., 2016, I : Clinical Genetics.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  40. Amplification and overexpression of Aurora kinase A (AURKA) in immortalized human ovarian epithelial (HOSE) cells

    Chung, C. M., Man, C., Jin, Y., Jin, C., Guan, X. Y., Wang, Q., Wan, T. S. K., Cheung, A. L. M. & Tsao, S. W., 2005, I : Molecular Carcinogenesis. 43, 3, s. 165-174

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  41. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.

    Collin, A., Povilas Sladkevicius & Soller, M., 2009, I : Prenatal Diagnosis. 29, s. 1279-1281

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  42. PKC activation sensitizes basal-like breast cancer cell lines to Smac mimetics

    Louise Cornmark, Christian Holmgren, Masoumi, K. & Christer Larsson, 2016, I : Cell death discovery. 2, s. 16002

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  43. Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

    Couch, F. J., Gaudet, M. M., Antoniou, A. C., Ramus, S. J., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., Wang, X., Kirchhoff, T., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Sinilnikova, O. M., Andrulis, I. L., Ozcelik, H., Mulligan, A. M., Thomassen, M., Gerdes, A-M. & 170 andraJensen, U. B., Skytte, A-B., Kruse, T. A., Caligo, M. A., von Wachenfeldt, A., Barbany-Bustinza, G., Niklas Loman, Soller, M., Hans Ehrencrona, Karlsson, P., Nathanson, K. L., Rebbeck, T. R., Domchek, S. M., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Zlowocka, E., Huzarski, T., Byrski, T., Gronwald, J., Cybulski, C., Górski, B., Osorio, A., Durán, M., Tejada, M. I., Benitez, J., Hamann, U., Hogervorst, F. B. L., van Os, T. A., van Leeuwen, F. E., Meijers-Heijboer, H. E. J., Wijnen, J., Blok, M. J., Kets, M., Hooning, M. J., Oldenburg, R. A., Ausems, M. G. E. M., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Jacobs, C., Eeles, R. A., Adlard, J., Davidson, R., Eccles, D. M., Cole, T., Cook, J., Paterson, J., Brewer, C., Douglas, F., Hodgson, S. V., Morrison, P. J., Walker, L., Porteous, M. E., Kennedy, M. J., Side, L. E., Bove, B., Godwin, A. K., Stoppa-Lyonnet, D., Fassy-Colcombet, M., Castera, L., Cornelis, F., Mazoyer, S., Léoné, M., Boutry-Kryza, N., Bressac-de Paillerets, B., Caron, O., Pujol, P., Coupier, I., Delnatte, C., Akloul, L., Lynch, H. T., Snyder, C. L., Buys, S. S., Daly, M. B., Terry, M., Chung, W. K., John, E. M., Miron, A., Southey, M. C., Hopper, J. L., Goldgar, D. E., Singer, C. F., Rappaport, C., Tea, M-K. M., Fink-Retter, A., Hansen, T. V. O., Nielsen, F. C., Arason, A., Vijai, J., Shah, S., Sarrel, K., Robson, M. E., Piedmonte, M., Phillips, K., Basil, J., Rubinstein, W. S., Boggess, J., Wakeley, K., Ewart-Toland, A., Montagna, M., Agata, S., Imyanitov, E. N., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Feliubadalo, L., Brunet, J., Gayther, S. A., Pharoah, P. P. D., Odunsi, K. O., Karlan, B. Y., Walsh, C. S., Olah, E., Teo, S. H., Ganz, P. A., Beattie, M. S., van Rensburg, E. J., Dorfling, C. M., Diez, O., Kwong, A., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Heidemann, S., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Fiebig, B., Heinritz, W., Caldes, T., de la Hoya, M., Muranen, T. A., Nevanlinna, H., Tischkowitz, M. D., Spurdle, A. B., Neuhausen, S. L., Ding, Y. C., Lindor, N. M., Fredericksen, Z., Pankratz, V. S., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Barile, M., Bernard, L., Viel, A., Giannini, G., Varesco, L., Radice, P., Greene, M. H., Mai, P. L., Easton, D. F., Chenevix-Trench, G., Offit, K. & Simard, J., 2012, I : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 21, 4, s. 645-657

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift