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المؤلفون: Dalmasso, B., Pastorino, L., Nathan, V., Shah, N.N., Palmer, J.M., Howlie, M., Johansson, P.A., Freedman, N.D., Carter, B.D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A.J., Helsing, P., Doorn, R. van, Gruis, N.A., Visser, M., Wadt, K.A.W., Mann, G., Holland, E.A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M.C., Calista, D., Soufir, N., Harland, M., Bishop, T., Kanetsky, P.A., Elder, D.E., Andreotti, V., Vanni, I., Bruno, W., Hoiom, V., Tucker, M.A., Yang, X.R., Andresen, P.A., Adams, D.J., Landi, M.T., Hayward, N.K., Goldstein, A.M., Ghiorzo, P., GenoMEL, MelaNostrum Consortia
المصدر: Genetics in Medicine, 23(11), 2087-2095. SPRINGERNATURE
Genetics in Medicine
Genetics in medicine : official journal of the American College of Medical Genetics, vol 23, iss 11مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Clinical Sciences, Ataxia Telangiectasia Mutated Proteins, MelaNostrum consortia, Article, Germline, Ataxia Telangiectasia, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Internal medicine, Genetics, medicine, 2.1 Biological and endogenous factors, Humans, Genetic Predisposition to Disease, Aetiology, Allele, Melanoma, Allele frequency, Exome, Genotyping, Germ-Line Mutation, Genetics (clinical), Cancer, Genetics & Heredity, business.industry, Human Genome, Australia, GenoMEL, medicine.disease, 030104 developmental biology, 030220 oncology & carcinogenesis, Ataxia-telangiectasia, Cohort, Settore MED/35 - MALATTIE CUTANEE E VENEREE, business
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51b0ef9606b12f87dff498e2a2603490
http://hdl.handle.net/1887/3280197 -
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