المؤلفون: Wadt, K. A. W., Aoude, L. G., Johansson, P., Solinas, A., Pritchard, A., Crainic, O., Andersen, M. T., Kiilgaard, J. F., Heegaard, S., Sunde, L., Federspiel, B., Madore, J., Thompson, J. F., McCarthy, S. W., Goodwin, A., Tsao, H., Jönsson, Göran B, Busam, K., Gupta, R., Trent, J. M., Gerdes, A. -M., Brown, K. M., Scolyer, R. A., Hayward, N. K.

المصدر: Clinical Genetics BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation. 88(3):267-272

مصطلحات موضوعية: BAP1, BCC, cancer predisposition syndrome, germline mutation, melanoma, unknown primary tumor, Medicin och hälsovetenskap, Klinisk medicin, Cancer och onkologi, Medical and Health Sciences, Clinical Medicine, Cancer and Oncology

الوصول الحر: https://lup.lub.lu.se/record/7975750Test
http://dx.doi.org/10.1111/cge.12501Test

المؤلفون: Wadt, K. A. W., Aoude, L. G., Krogh, Lotte Nylandsted, Sunde, L., Bojesen, A., Grønskov, K., Wartacz, N., Ek, J., Tolstrup-Andersen, M., Klarskov-Andersen, M., Borg, A., Heegaard, S., Kiilgaard, J. F., Hansen, T. V. O., Klein, K., Jonsson, G., Drzewiecki, K. T., Dunø, M., Hayward, N. K., Gerdes, A. M.

المصدر: Wadt , K A W , Aoude , L G , Krogh , L N , Sunde , L , Bojesen , A , Grønskov , K , Wartacz , N , Ek , J , Tolstrup-Andersen , M , Klarskov-Andersen , M , Borg , A , Heegaard , S , Kiilgaard , J F , Hansen , T V O , Klein , K , Jonsson , G , Drzewiecki , K T , Dunø , M , Hayward , N K & Gerdes , A M 2015 , ' Molecular Characterization of Melanoma Cases in Denmark ....

مصطلحات موضوعية: PANCREATIC-CANCER FAMILIES GENOME-WIDE ASSOCIATION POPULATION-BASED SAMPLE MITF GERMLINE MUTATION CUTANEOUS MELANOMA CDKN2A MUTATIONS UVEAL MELANOMA MC1R VARIANTS RISK-FACTORS SUSCEPTIBILITY GENE

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/e99f0331-dae2-4619-82f6-775699dfdbc1Test

الإتاحة: https://doi.org/10.1371/journal.pone.0122662Test
https://portal.findresearcher.sdu.dk/da/publications/e99f0331-dae2-4619-82f6-775699dfdbc1Test

المؤلفون: Wadt, K A W, Aoude, L G, Johansson, P, Solinas, A, Pritchard, A, Crainic, O, Andersen, M T, Kiilgaard, J F, Heegaard, S, Sunde, L, Federspiel, B, Madore, J, Thompson, J F, McCarthy, S W, Goodwin, A, Tsao, H, Jönsson, G, Busam, K, Gupta, R, Trent, J M, Gerdes, A-M, Brown, K M, Scolyer, R A, Hayward, N K

المصدر: Wadt, K A W, Aoude, L G, Johansson, P, Solinas, A, Pritchard, A, Crainic, O, Andersen, M T, Kiilgaard, J F, Heegaard, S, Sunde, L, Federspiel, B, Madore, J, Thompson, J F, McCarthy, S W, Goodwin, A, Tsao, H, Jönsson, G, Busam, K, Gupta, R, Trent, J M, Gerdes, A-M, Brown, K M, Scolyer, R A & Hayward, N K 2015, ' A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma ', Clinical Genetics, vol. 88, no. 3, pp. 267-72 . https://doi.org/10.1111/cge.12501Test

مصطلحات موضوعية: Male, Heterozygote, Tumor Suppressor Proteins, DNA Mutational Analysis, Loss of Heterozygosity, Polymorphism, Single Nucleotide, Pedigree, Haplotypes, Carcinoma, Basal Cell, Humans, Female, Genetic Predisposition to Disease, Ubiquitin Thiolesterase, Germ-Line Mutation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8683177f95e9340fad7ecbc1055bfad4Test
https://pubmed.ncbi.nlm.nih.gov/25225168Test