Výsledky vyhledávání - Maria Piane
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MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder Autor Domenico Delia, Maria Piane, Giacomo Buscemi, Camilla Savio, Silvia Palmeri, Patrizia Lulli, Luigi Carlessi, Enrico Fontanella, Luciana Chessa
Vydáno 2004Artigo -
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Genetic Testing and Clinical Management Practices for Variants in Non-<i>BRCA1</i>/<i>2</i> Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the... Autor Sarah M. Nielsen, Diana Eccles, Iris L. Romero, Fahd Al‐Mulla, Judith Balmañà, Michela Biancolella, Rien Blok, Maria A. Caligo, Mariarosaria Calvello, Gabriele Lorenzo Capone, Pietro Cavalli, Tai-Hua Chan, Kathleen Claes, Laura Cortesi, Fergus J. Couch, Miguel de la Hoya, Simona De Toffol, Orland Dı́ez, Susan M. Domchek, Rosalind A. Eeles, Anna Efremidis, Florentia Fostira, David E. Goldgar, Andreas Hadjisavvas, Thomas van Overeem Hansen, Akira Hirasawa, Claude Houdayer, Petra Kleiblová, Sophie Krieger, Conxi Lázaro, Maria A. Loizidou, Siranoush Manoukian, Arjen R. Mensenkamp, Setareh Moghadasi, Álvaro N.A. Monteiro, Luigi Mori, April Morrow, Nadia Naldi, Henriette Roed Nielsen, Olufunmilayo I. Olopade, Nicholas Pachter, Edenir Inêz Palmero, Inge Søkilde Pedersen, Maria Piane, Marianna Puzzo, Mark E. Robson, Maria Rossing, Maria Cristina Sini, Ángela R. Solano, Jana Soukupová, Gianluca Tedaldi, Manuel R. Teixeira, Mads Thomassen, Maria Grazia Tibiletti, Amanda E. Toland, Therese Törngren, Erica Vaccari, Liliana Varesco, Ana Vega, Yvonne Wallis, Barbara Wappenschmidt, Jeffrey N. Weitzel, Amanda B. Spurdle, Arcangela De Nicolo, E. Gómez
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Ataxia-telangiectasia
DNA
DNA damage
Genotype
Medicine
Neuroscience
Phenotype
Allele
Ataxia
Breast cancer
Cancer
Cancer research
Coronavirus disease 2019 (COVID-19)
DNA-binding protein
Disease
Etiology
Genetic testing
Heterozygote advantage
Hyposmia
Infectious disease (medical specialty)
Internal medicine
Mendelian inheritance
Molecular biology
Movement disorders
Mutation
Nijmegen breakage syndrome
Null allele