المؤلفون: Born, P W, Broholm, H, Laursen, H

المصدر: Ugeskrift for Laeger. 168(44):3813

المؤلفون: Tranebjaerg, L, Schrader, H, Paloneva, J

المصدر: Tidsskrift for Den Norske Laegeforening. 120(26):3196

المؤلفون: Stylianos E. Antonarakis, Ernst J Reichenberger, Alexander G. Marneros, Hamid Mehenni, T. Krieg, Bjorn R. Olsen

المصدر: Scopus-Elsevier
Cytogenetics and Cell Genetics, Vol. 92, No 3-4 (2001) pp. 213-216

مصطلحات موضوعية: Genetic Markers, congenital, hereditary, and neonatal diseases and abnormalities, Candidate gene, Mutation/genetics, DNA Mutational Analysis, Molecular Sequence Data, Peutz-Jeghers Syndrome/ genetics, Peutz-Jeghers Syndrome, STK11, Locus (genetics), Protein tyrosine phosphatase, Biology, Chromosomes, Human, Pair 19/ genetics, Contig Mapping, Genetic Heterogeneity, Exon, Gene mapping, Genetics, Humans, Disease-causing Mutation, RNA Splice Sites/genetics, skin and connective tissue diseases, Molecular Biology, Gene, Genetics (clinical), Sequence Tagged Sites, ddc:616, Genetic Markers/genetics, Introns/ genetics, Receptor-Like Protein Tyrosine Phosphatases, Class 3, Exons, Introns, Mutation, Protein Tyrosine Phosphatases/ genetics, RNA Splice Sites, Protein Tyrosine Phosphatases, Exons/ genetics, Chromosomes, Human, Pair 19

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::520955ac22c8a363f0d0a3c3ba6529a4Test
https://doi.org/10.1159/000056905Test

المؤلفون: Couch, F.J., Gaudet, M.M., Antoniou, A.C., Ramus, S.J., Kuchenbaecker, K.B., Soucy, P., Beesley, J., Chen, X.Q., Wang, X.S., 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., Jensen, U.B., Skytte, A.B., Kruse, T.A., Caligo, M.A., Wachenfeldt, A. von, Barbany-Bustinza, G., Loman, N., Soller, M., Ehrencrona, H., 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., Gorski, B., Osorio, A., Duran, M., Tejada, M.I., Benitez, J., Hamann, U., Hogervorst, F.B.L., Os, T.A. van, Leeuwen, F.E. van, 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., Leone, 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., Rensburg, E.J. van, 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., Hoya, M. de la, Muranen, T.A., Nevanlinna, H., Tischkowitz, M., 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., OCGN, SWE-BRCA, HEBON, EMBRACE, GEMO Study Collaborators, kConFab Investigators, Consortium Investigators Modifiers

المساهمون: European Commission, National Institutes of Health (US), Breast Cancer Research Foundation, Cancer Research UK, Columbia University, Fundación Mutua Madrileña, Asociación Española Contra el Cáncer, Ministerio de Ciencia e Innovación (España), National Institute for Health Research (UK), University of Helsinki, Generalitat de Catalunya, Instituto de Salud Carlos III, Ministero dell'Istruzione, dell'Università e della Ricerca, Ministero della Salute, National Health and Medical Research Council (Australia), Instituto Nacional del Cáncer (España), National Cancer Institute (US), Avon Foundation for Women, VU University medical center, Human genetics, CCA - Oncogenesis, Clinical Genetics, Pediatric Surgery, Neurology, Medical Oncology, MUMC+: DA KG Lab Centraal Lab (9), Genetica & Celbiologie, RS: GROW - School for Oncology and Reproduction, Human Genetics, CCA -Cancer Center Amsterdam, ARD - Amsterdam Reproduction and Development

المصدر: Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X Q, Wang, X S, 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, Jensen, U B, Skytte, A B, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, 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, Gorski, B, Osorio, A, Duran, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, Os, T A, van Leeuwen, F E, Meijers-Heijboer, E J, van 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, SV, 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, Leone, 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 2012, ' 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 ', Cancer Epidemiology Biomarkers and Prevention, vol. 21, no. 4, pp. 645-657 . https://doi.org/10.1158/1055-9965.EPI-11-0888Test
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, Jensen, U B, Skytte, A-B, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, 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 & OCGN 2012, ' 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 ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888Test
Cancer Epidemiology Biomarkers and Prevention, 21(4), 645-657. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention; Vol 21
Cancer Epidemiology, Biomarkers and Prevention, 21(4), 645-657
Cancer Epidemiology, Biomarkers & Prevention, 21, 4, pp. 645-57
Digital.CSIC. Repositorio Institucional del CSIC
instname
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 R, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A-M A, Jensen, U B, Skytte, A-B S, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P W, 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 & OCGN 2012, ' 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 ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888Test
Cancer Epidemiology Biomarkers & Prevention, 21(4), 645-657. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers & Prevention, 21, 645-57
Cancer epidemiology, biomarkers & prevention, 21(4), 645-657. American Association for Cancer Research Inc.

مصطلحات موضوعية: Oncology, endocrine system diseases, Epidemiology, Estrogen receptor, Breast Neoplasms - epidemiology - genetics - metabolism, DCN PAC - Perception action and control, Immunoenzyme Techniques, 0302 clinical medicine, Risk Factors, Genotype, skin and connective tissue diseases, Ovarian Neoplasms, 0303 health sciences, Ovarian Neoplasms - epidemiology - genetics - metabolism, BRCA1 Protein, Middle Aged, BRCA2 Protein, Prognosis, 3. Good health, DNA-Binding Proteins, Receptors, Estrogen, Risk factors for breast cancer, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Female, Adult, medicine.medical_specialty, Hereditary cancer and cancer-related syndromes Genetics and epigenetic pathways of disease [ONCOL 1], Breast Neoplasms, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Breast cancer, SDG 3 - Good Health and Well-being, Translational research [ONCOL 3], Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], 030304 developmental biology, Aged, Chromosomes, Human, Pair 19 - genetics, Hereditary cancer and cancer-related syndromes [ONCOL 1], business.industry, Cancer, BRCA1 Protein - genetics, medicine.disease, United States, BRCA2 Protein - genetics, Immunology, Mutation, Ovarian cancer, business, Chromosomes, Human, Pair 19, Genome-Wide Association Study, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b949799806fed1689a9d24c254b3c62Test
https://research.vumc.nl/en/publications/f7b6f7f2-aac8-4050-a221-f53efa006269Test

المؤلفون: Marie-Magdeleine Ruchoux, Jacqueline Mikol, Isabelle Salmon, Dominique Figarella-Branger, David W. Ellison, Emmanuel Rousseau, Francesco Scaravilli, Catherine Lacroix, Thomas Palm, Catherine Godfraind, Miikka Vikkula, Françoise Chapon

المساهمون: UCL - MD/MNOP - Département de morphologie normale et pathologique, UCL - MD/BICL - Département de biochimie et de biologie cellulaire, UCL - (SLuc) Service d'anatomie pathologique, UCL - (SLuc) Centre de génétique médicale UCL, UCL - (SLuc) Centre de malformations vasculaires congénitales

المصدر: Molecular Cancer, Vol 6, Iss 1, p 47 (2007)
Molecular Cancer, Vol. 6, p. 47 [1-10] (2007)
Molecular Cancer
Molecular cancer, 6

مصطلحات موضوعية: Ependymoma, Chromosomes, Human, Pair 11 -- genetics, Microsatellite Repeats -- genetics, Male, Pathology, Cancer Research, Tissue Fixation, Trisomy, medicine.disease_cause, Chromosomes, Human, Pair 19 -- genetics, Child, Glial fibrillary acidic protein, biology, Brain Neoplasms, Nucleic Acid Hybridization, Sciences bio-médicales et agricoles, Middle Aged, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Oncology, Child, Preschool, Molecular Medicine, Female, Chromosome Deletion, Ependymoma -- pathology, Chromosomes, Human, Pair 9, Adult, medicine.medical_specialty, Adolescent, Chromosome 9, Brain Neoplasms -- genetics, Polymorphism, Single Nucleotide, lcsh:RC254-282, Brain Neoplasms -- pathology, Chromosome 19, medicine, Humans, Tissue Array Analysis -- methods, Ependymoma -- genetics, Aged, Genome, Human, Research, Chromosomes, Human, Pair 11, Infant, Tissue Fixation -- methods, medicine.disease, Nucleic Acid Hybridization -- methods, Tissue Array Analysis, biology.protein, Human genome, Carcinogenesis, Chromosomes, Human, Pair 9 -- genetics, Chromosomes, Human, Pair 19, Clear cell, Microsatellite Repeats

وصف الملف: 1 full-text file(s): application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af54cbe2d2dac6f2f69f1a8c767f0baTest
http://www.molecular-cancer.com/content/6/1/47Test

المؤلفون: Vang Nielsen, K, Bruun Rasmussen, B, Balslev, E, Svenstrup Poulsen, T, Schönau, A, Ejlertsen, B

المصدر: Ugeskrift for Laeger. 169(2):147

المؤلفون: S Gorezis, Kang Zhang, Michael B. Petersen, Maria Grigoriadou, Marielle Payne, Yu Zhao, George Kitsos, Zhenglin Yang, K. Psilas, Shin Kamaya, G. Aperis, Zongzhong Tong

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Genotype, Genetic Linkage, Haplotypes/genetics, Locus (genetics), Biology, Electronic Letter, Genes, Dominant/*genetics, Macular Degeneration, Chromosomes, Human, Pair 19/*genetics, Genetic linkage, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetics (clinical), Aged, Genes, Dominant, Genetic Linkage/genetics, Aged, 80 and over, Family Health, Greece, Genome, Human, Haplotype, Macular Degeneration/*genetics/pathology, Genetic Predisposition to Disease/*genetics, Macular degeneration, Macular dystrophy, Middle Aged, medicine.disease, Pedigree, Haplotypes, Genome, Human/genetics, Medical genetics, Microsatellite, Female, Lod Score, Chromosomes, Human, Pair 19, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cab8642894f47986a1dc7d5cc80e7951Test
https://europepmc.org/articles/PMC2563205Test/

المؤلفون: Öksengård, A R, Engedal, K

المصدر: Tidsskrift for Den Norske Laegeforening. 122(5):530

المؤلفون: Kent F. Richards, V.B. Dixit, Ambrosio Bermejo-Fenoll, Jean-Louis Blouin, Kamla Bhardwaj, Ranjan C. Raval, Uppala Radhakrishna, Shiv Shanker Bhardwaj, Hamid Mehenni, Antonio Silva Leal, Stylianos E. Antonarakis

المصدر: American Journal of Human Genetics, Vol. 61, No 6 (1997) pp. 1327-1334

مصطلحات موضوعية: Genetic Markers, Male, congenital, hereditary, and neonatal diseases and abnormalities, Positional cloning, Peutz-Jeghers Syndrome, Peutz-Jeghers Syndrome/ genetics, Peutz–Jeghers syndrome, Locus (genetics), Biology, DNA/genetics, Chromosomes, Human, Pair 19/ genetics, Gene mapping, Genetic linkage, medicine, Genetics, Humans, Genetics(clinical), Allele, Cloning, Molecular, skin and connective tissue diseases, Genetics (clinical), Alleles, Cancer, intestinal, Genes, Dominant, ddc:616, Polymorphism, Genetic, Autosomal dominant trait, Chromosome Mapping, Chromosome 19, DNA, medicine.disease, Penetrance, Neoplasias, Pedigree, Female, Lod Score, Chromosomes, Human, Pair 19, Linkage analysis, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2139d5fc6c09b0650e7e8acf49c6796Test
https://archive-ouverte.unige.ch/unige:8890Test

المؤلفون: Catherine Ucla, Lisa Stubbs, Bernard Mach, Susan M.G. Hoffman, Johannah Doyle, Walter Reith

المصدر: Genomics, Vol. 35, No 1 (1996) pp. 227-230

مصطلحات موضوعية: TBX1, Genetic Linkage, Molecular Sequence Data, DNA-Binding Proteins/ genetics, Regulatory Factor X Transcription Factors, ddc:616.07, Biology, DNA sequencing, Chromosomes, Human, Pair 19/ genetics, Mice, chemistry.chemical_compound, Genes, jun, Gene mapping, Chromosome 19, Mice/ genetics, Muridae/genetics, Genetics, Animals, Humans, Gene family, Gene, Crosses, Genetic, In Situ Hybridization, Base Sequence, Transcription Factors/ genetics, Linkage (Genetics), Chromosome Mapping, DNA-binding domain, DNA-Binding Proteins, Muridae, Genes, chemistry, Multigene Family, Regulatory Factor X1, Chromosomes, Human, Pair 19, DNA, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1176e6d18fdce28d542a7c97fc71f799Test
https://zenodo.org/record/1229693Test