From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.
JAMA oncology 2016 Dec .
Neidhardt Guido, Hauke Jan, Ramser Juliane, Groß Eva, Gehrig Andrea, Müller Clemens R, Kahlert Anne-Karin, Hackmann Karl, Honisch Ellen, Niederacher Dieter, Heilmann-Heimbach Stefanie, Franke André, Lieb Wolfgang, Thiele Holger, Altmüller Janine, Nürnberg Peter, Klaschik Kristina, Ernst Corinna, Ditsch Nina, Jessen Frank, Ramirez Alfredo, Wappenschmidt Barbara, Engel Christoph, Rhiem Kerstin, Meindl Alfons, Schmutzler Rita K, Hahnen Er - Association between basal-like phenotype and BRCA1/2 germline mutations in Korean breast cancer patients.
Current oncology (Toronto, Ont.) 2016 Oct 23 (5): 298-303.
Jung J, Kang E, Gwak J M, Seo A N, Park S Y, Lee A S, Baek H, Chae S, Kim E K, Kim S - Early onset breast cancer in Ashkenazi women carriers of founder BRCA1/2 mutations: beyond 10 years of follow-up.
European journal of cancer care 2016 Oct .
Dagan E, Gershoni-Baruch R, Kurolap A, Fried - Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry.
Oncotarget 2016 Oct .
Fernandes Gabriela C, Michelli Rodrigo Ad, Galvão Henrique Cr, Paula André E, Pereira Rui, Andrade Carlos E, Felicio Paula S, Souza Cristiano P, Mendes Deise Rp, Volc Sahlua, Berardinelli Gustavo N, Grasel Rebeca S, Sabato Cristina S, Viana Danilo V, Mauad Edmundo C, Scapulatempo-Neto Cristovam, Arun Banu, Reis Rui M, Palmero Edenir - Whole-exome sequencing of Finnish hereditary breast cancer families.
European journal of human genetics : EJHG 2016 Oct .
Määttä Kirsi, Rantapero Tommi, Lindström Anna, Nykter Matti, Kankuri-Tammilehto Minna, Laasanen Satu-Leena, Schleutker Johan
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