المؤلفون: Silva, Amanda G.¹ amandagonc@yahoo.com, Krepischi, Ana C. V.^1,2 ana.krepischi@gmail.com, Pearson, Peter L.¹ peterlpearson@uol.com.br, Hainaut, Pierre³ hainautpierre@aol.com, Rosenberg, Carla¹ carlarosenberg@uol.com.br, Achatz, Maria Isabel⁴ miachatz@gmail.com

المصدر: Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p1-15. 15p.

مصطلحات موضوعية: *LI-Fraumeni syndrome, *GERM cells, *TUMOR suppressor genes, *CANCER risk factors, *P53 protein, *GENETIC disorders, *PATIENTS

المؤلفون: Silva, Amanda G.¹, Isabel W. Achatz, Maria¹, V. Krepischi, Ana C.¹, Pearson, Peter L.², Rosenberg, Carla² carlarosenberg@uol.com.br

المصدر: Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p101-106. 6p. 2 Charts, 1 Graph.

مصطلحات موضوعية: *LI-Fraumeni syndrome, *CANCER patients, *TUMORS, *ONCOLOGY, *CYSTS (Pathology)

المؤلفون: Maria Isabel Achatz, Ana Cv Krepischi, Carla Rosenberg, Amanda Gonçalves Silva, Peter L. Pearson

المصدر: Orphanet Journal of Rare Diseases
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 101 (2012)

مصطلحات موضوعية: Male, DNA Copy Number Variations, Genotype, CNV, lcsh:Medicine, Penetrance, Biology, Germline, Li-Fraumeni Syndrome, Germline mutation, medicine, Humans, Genetics(clinical), Pharmacology (medical), Copy-number variation, TP53, Genetics (clinical), Germ-Line Mutation, Medicine(all), Genetics, Research, lcsh:R, General Medicine, medicine.disease, Human genetics, R337H, Li–Fraumeni syndrome, NEOPLASIAS, Mutation (genetic algorithm), Female, Tumor Suppressor Protein p53, Brazil

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22356e074ed6c64007685ca3692009eTest
http://europepmc.org/articles/PMC3558401Test