المؤلفون: Linda A. J. Hendricks, Katja C. J. Verbeek, Janneke H. M. Schuurs-Hoeijmakers, Arjen R. Mensenkamp, Hilde Brems, Robin de Putter, Violetta C. Anastasiadou, Marie-Charlotte Villy, Arne Jahn, Verena Steinke-Lange, Margherita Baldassarri, Arvids Irmejs, Mirjam M. de Jong, Thera P. Links, Edward M. Leter, Daniëlle G. M. Bosch, Hildegunn Høberg-Vetti, Marianne Tveit Haavind, Kjersti Jørgensen, Lovise Mæhle, Ana Blatnik, Joan Brunet, Esther Darder, Emma Tham, Nicoline Hoogerbrugge, Janet R. Vos

المصدر: Cancers, Vol 16, Iss 5, p 953 (2024)

مصطلحات موضوعية: alcohol drinking, body mass index, breast neoplasm, exercise, hamartoma syndrome, multiple, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2072-6694/16/5/953Test; https://doaj.org/toc/2072-6694Test

الوصول الحر: https://doaj.org/article/fec7f542d3f149ddb920a8ada25386b8Test

المؤلفون: Iris B.A.W. Te Paske, Arjen R. Mensenkamp, Kornelia Neveling, Nicoline Hoogerbrugge, Marjolijn J.L. Ligtenberg, Richarda M. De Voer, Stéphanie Baert-Desurmont, Kathleen B.M. Claes, Kim de Leeneer, Lisa Elze, Simone van den Heuvel, Rachel S. van der Post, Yvonne van Twuijver, Tjakko J. van Ham, Anja Wagner, Mirjam M. de Jong, Edward M. Leter, Maartje Nielsen

المساهمون: MUMC+: DA KG Polikliniek (9), RS: FHML non-thematic output

المصدر: Gastroenterology, 163, 1691-1694.e7
GASTROENTEROLOGY
Gastroenterology, 163, 6, pp. 1691-1694.e7
Gastroenterology, 163(6), 1691-1694.e7. Elsevier Saunders

مصطلحات موضوعية: Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Hereditary Nonpolyposis/diagnosis, Hepatology, Gastroenterology, Biology and Life Sciences, DNA Mismatch Repair/genetics, DNA Mismatch Repair, Colorectal Neoplasms, Hereditary Nonpolyposis, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Medicine and Health Sciences, Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis, Humans, Colorectal Neoplasms

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6ca06207cc896da6e4c3a143fba3cccTest
https://research.rug.nl/en/publications/951dee72-4ac1-4836-920f-73b753838cf8Test

المؤلفون: Linda A.J. Hendricks, Nicoline Hoogerbrugge, Hanka Venselaar, Stefan Aretz, Isabel Spier, Eric Legius, Hilde Brems, Robin de Putter, Kathleen B.M. Claes, D. Gareth Evans, Emma R. Woodward, Maurizio Genuardi, Fulvia Brugnoletti, Yvette van Ierland, Kim Dijke, Emma Tham, Bianca Tesi, Janneke H.M. Schuurs-Hoeijmakers, Maud Branchaud, Hector Salvador, Arne Jahn, Simon Schnaiter, Violetta Christophidou Anastasiadou, Joan Brunet, Carla Oliveira, Laura Roht, Ana Blatnik, Arvids Irmejs, Arjen R. Mensenkamp, Janet R. Vos, Floor Duijkers, Jacques C. Giltay, Liselotte P. van Hest, Tjitske Kleefstra, Edward M. Leter, Maartje Nielsen, Sebastiaan W.R. Nijmeijer, Maran J.W. Olderode-Berends

المساهمون: Human genetics, Cancer Center Amsterdam, CCA - Cancer biology and immunology, Clinical Genetics, MUMC+: DA KG Polikliniek (9), RS: FHML non-thematic output

المصدر: European Journal of Medical Genetics, 65(12):104632. Elsevier Masson SAS
European journal of medical genetics, 65(12):104632. ELSEVIER SCIENCE BV
European Journal of Medical Genetics, 65(12):104632. Elsevier Masson
EUROPEAN JOURNAL OF MEDICAL GENETICS
European Journal of Medical Genetics, 65, 12
PTEN Study Group 2022, ' Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort ', European Journal of Medical Genetics, vol. 65, no. 12, 104632 . https://doi.org/10.1016/j.ejmg.2022.104632Test
European Journal of Medical Genetics, 65(12). Elsevier
European Journal of Medical Genetics, 65

مصطلحات موضوعية: Genetic association studies, Medical oncology, Oncologia, Hamartoma, Settore MED/03 - GENETICA MEDICA, Hamartoma Syndrome, Cohort Studies, Tumours of the digestive tract Radboud Institute for Health Sciences [Radboudumc 14], All institutes and research themes of the Radboud University Medical Center, Human genetics, SDG 3 - Good Health and Well-being, Medical, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Medicine and Health Sciences, Genetics, Humans, Genetic variation, AUTISM, Hamartoma Syndrome, Multiple/genetics, Genetics (clinical), SPECTRUM, Genètica humana, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], MUTATIONS, PTEN Phosphohydrolase, Biology and Life Sciences, PTEN Phosphohydrolase/genetics, General Medicine, COWDEN-DISEASE, CANCER, Megalencephaly, RISKS, Fenotip, Phenotype, oncology, Multiple/genetics, Megalencephaly/genetics, Hamartoma Syndrome, Multiple, Nanomedicine Radboud Institute for Molecular Life Sciences [Radboudumc 19]

وصف الملف: application/pdf; Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b579f2ee726b8aee2834cd899346baeTest
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/285925Test

المؤلفون: Janet R. Vos, Sera Langenveld, Liesbeth Spruijt, Ingrid E Fakkert, Edward M Leter, Marjolijn J. L. Ligtenberg, Arjen R. Mensenkamp, Riki W. Willems, Nicoline Hoogerbrugge, Iris D. Nagtegaal

المساهمون: MUMC+: DA KG Polikliniek (9), RS: FHML non-thematic output

المصدر: International Journal of Cancer
International Journal of Cancer, 147, 2150-2158
International Journal of Cancer, 147, 8, pp. 2150-2158
International Journal of Cancer, 147(8), 2150-2158. Wiley

مصطلحات موضوعية: Male, Oncology, Cancer Research, Cancer Genetics And Epigenetics, Colorectal cancer, diagnosis, germline, DNA Mismatch Repair, Germline, Tumours of the digestive tract Radboud Institute for Health Sciences [Radboudumc 14], 0302 clinical medicine, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], somatic mutation, Prospective Studies, guidelines, Promoter Regions, Genetic, Prospective cohort study, risk, mechanisms, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], medicine.diagnostic_test, Middle Aged, Lynch syndrome, germline mutation, mlh1, 030220 oncology & carcinogenesis, Female, DNA mismatch repair, recognition, Colorectal Neoplasms, MutL Protein Homolog 1, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, colorectal cancer, MLH1, Young Adult, 03 medical and health sciences, Germline mutation, Internal medicine, medicine, Humans, Genetic Testing, neoplasms, Aged, Genetic testing, business.industry, mismatch repair deficiency, DNA Methylation, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Mutation, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b685957977e871f78f34fcb5896bfd22Test
http://europepmc.org/articles/PMC7496272Test

المؤلفون: Antonius F.W. van Hout, Jasper J. van der Smagt, Cora M. Aalfs, Klara Mosterd, M.G.H.C. Reinders, Edward M. Leter, Frederik J. Hes, Lieke P.V. Berger, Anja Wagner, C. Marleen Kets, Lizet E. van der Kolk, Johan J.P. Gille, Michel van Geel, Peter M. Steijlen, B. Cosgun, Johanna M. van Hagen

المساهمون: Clinical Genetics, Clinical sciences, Medical Genetics, Human genetics, Amsterdam Reproduction & Development (AR&D), MUMC+: MA AIOS Dermatologie (9), RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Dermatologie, MUMC+: MA Dermatologie (9), MUMC+: DA KG Lab Centraal Lab (9), MUMC+: MA Dermatologie (3), MUMC+: CONC Poli Dermatologie (9), MUMC+: DA KG Polikliniek (9), Academic Medical Center

المصدر: Journal of the American Academy of Dermatology, 83(2), 604-607. Mosby Inc.
Journal of the American Academy of Dermatology, 83(2), 604-607. MOSBY-ELSEVIER
Journal of the American Academy of Dermatology, 83, 604-607
Journal of the American Academy of Dermatology, 83, 2, pp. 604-607
Cosgun, B, Reinders, M G H C, van Geel, M, Steijlen, P M, van Hout, A F W, Leter, E M, van der Smagt, J J, van Hagen, J M, Berger, L P V, Kets, C M, Wagner, A, Aalfs, C M, Hes, F J, van der Kolk, L E, Gille, J J P & Mosterd, K 2020, ' Lack of genotype-phenotype correlation in basal cell nevus syndrome : A Dutch multicenter retrospective cohort study ', Journal of the American Academy of Dermatology, vol. 83, no. 2, pp. 604-607 . https://doi.org/10.1016/j.jaad.2019.07.072Test

مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, PTCH1, SUFU, DNA Mutational Analysis, Basal Cell Nevus Syndrome, MEDLINE, Dermatology, heat map, medulloblastoma, Genotype phenotype, basal cell carcinoma, Internal medicine, medicine, Humans, Basal cell carcinoma, basal cell nevus syndrome, Genetic Association Studies, Netherlands, Retrospective Studies, Medulloblastoma, Medicine(all), business.industry, Retrospective cohort study, medicine.disease, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], Gorlin syndrome, genotype-phenotype, Patched-1 Receptor, odontogenic keratocyst, diagnostic criteria, Female, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f93cdbdeb380566cfa1fd0a80693af26Test
https://doi.org/10.1016/j.jaad.2019.07.072Test

المؤلفون: Lisa Elze, Arjen R. Mensenkamp, Iris D. Nagtegaal, Wendy A.G. van Zelst-Stams, Richarda M. de Voer, Marjolijn J.L. Ligtenberg, Charlotte J. Dommering, Nicoline Hoogerbrugge, Mirjam M. de Jong, Fonnet E. Bleeker, Edward M. Leter, Tom G.W. Letteboer, Maartje Nielsen, Rachel S. van der Post, Brigit Wapstra

المصدر: Dutch LS-Like Study Group 2021, ' Somatic Nonepigenetic Mismatch Repair Gene Aberrations Underly Most Mismatch Repair–Deficient Lynch-Like Tumors ', Gastroenterology, vol. 160, no. 4, pp. 1414-1416.e3 . https://doi.org/10.1053/j.gastro.2020.11.042Test
Gastroenterology, 160, 4, pp. 1414-1416.e3
Gastroenterology, 160, 1414-1416.e3

مصطلحات موضوعية: Adult, Male, Adolescent, Colorectal cancer, Somatic cell, DNA Mutational Analysis, DNA Mismatch Repair, Cohort Studies, Young Adult, Prevalence, medicine, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Humans, Multiplex ligation-dependent probe amplification, Gene, Aged, Netherlands, Aged, 80 and over, Molecular Epidemiology, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], Hepatology, business.industry, Endometrial cancer, Metabolic Disorders Radboud Institute for Health Sciences [Radboudumc 6], Gastroenterology, Microsatellite instability, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Mutation, Cancer research, Female, Microsatellite Instability, DNA mismatch repair, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a6d37d7fca938eb321ef59c4b32d4d3Test
https://research.vumc.nl/en/publications/37d763d2-9179-46a1-8ab4-5da52167446cTest

المؤلفون: Klara Mosterd, B. Cosgun, Johan J.P. Gille, P.M. Steijlen, Antonius F. van Hout, Aimee D C Paulussen, Michel van Geel, Edward M Leter, M.G.H.C. Reinders

المساهمون: RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Promovendi ODB, Dermatologie, MUMC+: MA Dermatologie (9), MUMC+: DA KG Lab Centraal Lab (9), MUMC+: DA KG Polikliniek (9), MUMC+: MA Dermatologie (3), MUMC+: MA AIOS Dermatologie (9), Human genetics, CCA - Cancer biology and immunology

المصدر: Reinders, M G, van Hout, A F, Cosgun, B, Paulussen, A D, Leter, E M, Steijlen, P M, Mosterd, K, van Geel, M & Gille, J J 2018, ' New mutations and an updated database for the patched-1 (PTCH1) gene ', Molecular Genetics and Genomic Medicine, vol. 6, no. 3, pp. 409-415 . https://doi.org/10.1002/mgg3.380Test
Molecular genetics & genomic medicine, 6(3), 409-415. Wiley
Molecular Genetics and Genomic Medicine, 6(3), 409-415. John Wiley and Sons Inc.
Molecular Genetics & Genomic Medicine

مصطلحات موضوعية: Patched Receptors, 0301 basic medicine, endocrine system, PTCH1, DNA Mutational Analysis, Basal Cell Nevus Syndrome, PROTEIN, Receptors, Cell Surface, medicine.disease_cause, computer.software_genre, BASAL-CELL CARCINOMA, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Holoprosencephaly, Databases, Genetic, Genetics, medicine, Humans, Molecular Biology, Germ-Line Mutation, Genetics (clinical), GORLIN SYNDROME, Mutation, Database, business.industry, Basal cell nevus syndrome, mutation database, NEVUS SYNDROME, Original Articles, PTCH1 Gene, medicine.disease, Patched-1 Receptor, 030104 developmental biology, MEDULLOBLASTOMA, 030220 oncology & carcinogenesis, Mutation testing, Original Article, Leiden Open Variation Database, business, computer, BCNS

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::473330b6b283652cb298743fe7ef63deTest
https://research.vumc.nl/en/publications/3051f4fd-dac4-43ff-9d58-fe7fba466867Test

المؤلفون: Henricus P. M. Kunst, Mirjam M. de Jong, Bernadette M P van Nesselrooij, Frederik J. Hes, Henri J L M Timmers, Arjen R. Mensenkamp, Edward M Leter, Hans Morreau, Benno Küsters, Winand N.M. Dinjens, Anouk N A van de Horst-Schrivers, Karin van der Tuin, Jeroen C. Jansen, Eleonora P M Corssmit, Liesbeth Spruijt, Carli M. J. Tops, Rogier A. Oldenburg

المساهمون: Pathology, Clinical Genetics, Medical Genetics, Guided Treatment in Optimal Selected Cancer Patients (GUTS), MUMC+: DA KG Polikliniek (9), RS: FHML non-thematic output

المصدر: Journal of Clinical Endocrinology and Metabolism, 103, 438-445
Journal of Clinical Endocrinology and Metabolism, 103(2), 438-445. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 103, 2, pp. 438-445
Journal of Clinical Endocrinology and Metabolism, 103(2), 438. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 103(2), 438-445
Journal of Clinical Endocrinology & Metabolism, 103(2), 438-445. ENDOCRINE SOC
Journal of Clinical Endocrinology & Metabolism, 103(2), 438-445. Oxford University Press

مصطلحات موضوعية: Male, Oncology, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Clinical Biochemistry, Adrenal Gland Neoplasms, SDHA, Penetrance, Paraganglioma/epidemiology, Biochemistry, Germline, 0302 clinical medicine, Endocrinology, Paraganglioma, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Medicine, Child, Netherlands, Medicine(all), Electron Transport Complex II, GASTROINTESTINAL STROMAL TUMORS, Vascular damage Radboud Institute for Molecular Life Sciences [Radboudumc 16], Middle Aged, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Pheochromocytoma/epidemiology, 030220 oncology & carcinogenesis, Electron Transport Complex II/genetics, young adult, Female, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Adult, medicine.medical_specialty, GENES, Adolescent, Genetic counseling, SOCIETY, Netherlands/epidemiology, 030209 endocrinology & metabolism, Context (language use), Pheochromocytoma, Adrenal Gland Neoplasms/epidemiology, 03 medical and health sciences, Germline mutation, All institutes and research themes of the Radboud University Medical Center, Internal medicine, Humans, Genetic Predisposition to Disease, HEAD, Germ-Line Mutation, Aged, Retrospective Studies, business.industry, MUTATIONS, Biochemistry (medical), medicine.disease, NECK PARAGANGLIOMAS, PRACTICE GUIDELINE, aged, 80 and over, business

وصف الملف: image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e637f8a4bc71e337012c3145db1d350eTest
http://hdl.handle.net/2066/184000Test

المؤلفون: Tsun Leung Chan, Eugène T P Verwiel, Irma Kluijt, Diana Eccles, Rolf H. Sijmons, Egbert J.W. Redeker, Rachel S. van der Post, Encarna B. Gomez Garcia, Reinhard Büttner, Cora M. Aalfs, Roland P. Kuiper, Johan J.P. Gille, Bernadette P M van Nesselrooij, Frans B. L. Hogervorst, Marjolijn J L Ligtenberg, Tracy Graham, Julie O. Culver, Edith Olah, Monique Goossens, Carli M. J. Tops, Elke Holinski-Feder, David J. Bunyan, Marielle E. van Gijn, Frederik J. Hes, Suet Yi Leung, Pierre O. Chappuis, Monika Morak, Edward M Leter, Nils Rahner, Lea Velsher, János Papp, Renee C. Niessen, J. Han van Krieken, Lambertus A. Kiemeney, Ad Geurts van Kessel, Charlotte W. Ockeloen, Nicoline Hoogerbrugge, Marlies Kempers, Iris D. Nagtegaal, Verena Steinke, Hans K. Schackert, Matthias Kloor, Melanie R. Palomares, Sapna Syngal, Pierre Hutter, Elena M. Stoffel

المساهمون: Genetica & Celbiologie, RS: GROW - School for Oncology and Reproduction, Clinical sciences, Human Genetics, ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Human genetics, CCA - Oncogenesis

المصدر: Kempers, M J E, Kuiper, R P, Ockeloen, C W, Chappuis, P O, Hutter, P, Rahner, N, Schackert, H K, Steinke, V, Holinski-Feder, E, Morak, M, Kloor, M, Buttner, R, Verwiel, E T P, van Krieken, J H, Nagtegaal, I D, Goossens, M, van der Post, R S, Niessen, R C, Sijmons, RH, Kluijt, I, Hogervorst, F B L, Leter, E M, Gille, J J P, Aalfs, C M, Redeker, E J W, Hes, F J, Tops, C M J, van Nesselrooij, B P M, van Gijn, M E, Garcia, E B G, Eccles, D M, Bunyan, D J, Syngal, S, Stoffel, E M, Culver, J O, Palomares, M R, Graham, T, Velsher, L, Papp, J, Olah, E, Chan, T L, Leung, S Y, van Kessel, A G, Kiemeney, L A L M, Hoogerbrugge, N & Ligtenberg, M J L 2011, ' Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study ', Lancet Oncology, vol. 12, no. 1, pp. 49-55 . https://doi.org/10.1016/S1470-2045Test(10)70265-5
The Lancet Oncology, 49-55
STARTPAGE=49;ENDPAGE=55;TITLE=The Lancet Oncology
Lancet Oncology, 12, 1, pp. 49-55
Lancet oncology, 12(1), 49-55. Elsevier Science
Lancet Oncology, 12, 49-55
lancet oncology, 12(1), 49-55. Lancet Publishing Group
Lancet Oncology, 12(1), 49-55. ELSEVIER SCIENCE INC
Lancet Oncology, 12(1), 49-55. Lancet Publishing Group

مصطلحات موضوعية: Male, Oncology, Genetics and epigenetic pathways of disease [NCMLS 6], REPAIR GENE HMSH2, Colorectal cancer, FAMILIES, chemistry.chemical_compound, Promoter Regions, Genetic, Colorectal Neoplasms/etiology, risk, Sequence Deletion, Medicine(all), METHYLATION, Epithelial cell adhesion molecule, Middle Aged, Epithelial Cell Adhesion Molecule, Translational research Tissue engineering and pathology [ONCOL 3], Lynch syndrome, Antigens, Neoplasm/genetics, Endometrial Neoplasms/etiology, MutS Homolog 2 Protein, Cohort studies, Female, Duodenal cancer, Colorectal Neoplasms, Cell Adhesion Molecules/genetics, STEM-CELLS, MutS Homolog 2 Protein/genetics, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, TACSTD1, Hereditary cancer and cancer-related syndromes Genetics and epigenetic pathways of disease [ONCOL 1], MUTATION CARRIERS, MLH1, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Antigens, Neoplasm, Translational research [ONCOL 3], Internal medicine, SURVEILLANCE, medicine, MANAGEMENT, Humans, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], neoplasms, Aged, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Gynecology, Hereditary cancer and cancer-related syndromes [ONCOL 1], business.industry, Endometrial cancer, Cancer, nutritional and metabolic diseases, medicine.disease, HYPERMETHYLATION, digestive system diseases, Endometrial Neoplasms, MSH2, MSH6, chemistry, business, Cell Adhesion Molecules, Gene Deletion

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f4a39c0f97e31d38f52cdcda56a8a1Test
https://hdl.handle.net/2066/97324Test

المؤلفون: Elisabeth H Jaspars, N.C.T. van Grieken, M. B. A. van Doorn, Edward M Leter, Ernie M.H.F. Bongers, Paul C Johannesma, Pieter E. Postmus, Lieke Gijezen, J-H T. M. van Waesberghe, Theo M. Starink, M.A.M. van Steensel, Arjan C. Houweling, Rogier A. Oldenburg, R.J.A. Van Moorselaar, Marianne A. Jonker, T. A. M. van Os, Johan J.P. Gille, K. Y. van Spaendonck-Zwarts, M. M. de Jong, Fred H. Menko

المساهمون: Stochastics, Mathematics, Human Genetics, Dermatologie, RS: GROW - School for Oncology and Reproduction, Human genetics, Dermatology, Pathology, Pulmonary medicine, Urology, Radiology and nuclear medicine, CCA - Oncogenesis

المصدر: British Journal of Cancer, 105(12), 1912-1919. Nature Publishing Group
Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A M, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J H T M, Starink, T M, van Steensel, M A M, Gille, J J P & Menko, F H 2011, ' Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families ', British Journal of Cancer, vol. 105, no. 12, pp. 1912-1919 . https://doi.org/10.1038/bjc.2011.463Test
British Jounal of Cancer, 105(12), 1912-1919. Nature Publishing Group
British Journal of Cancer
British journal of cancer, 105(12), 1912-1919. Nature Publishing Group

مصطلحات موضوعية: Adult, Male, Oncology, Cancer Research, medicine.medical_specialty, Pathology, pneumothorax, discoid fibroma, fibrofolliculoma, renal cancer, folliculin, Disease, TRICHODISCOMAS, Birt–Hogg–Dubé syndrome, SDG 3 - Good Health and Well-being, GENE FLCN, Proto-Oncogene Proteins, Internal medicine, Eosinophilic, medicine, MANAGEMENT, Humans, Genetic Predisposition to Disease, Birt-Hogg-Dube syndrome, Folliculin, Aged, SPECTRUM, business.industry, Tumor Suppressor Proteins, Cancer, Genetics and Genomics, LUNG CYSTS, ADULTS, Middle Aged, CELL CARCINOMA, medicine.disease, Penetrance, TUMORS, Kidney Neoplasms, Pneumothorax, Mutation, Female, business, Clear cell

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee60ff288397312c36a9973e0efd5722Test
https://doi.org/10.1038/bjc.2011.463Test