Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Variant , Quest Diagnostics"'
Autor:
Béroud , Christophe, Letovsky , Stanley I., Braastad , Corey D., Caputo , Sandrine M., Beaudoux , Olivia, Bignon , Yves Jean, Paillerets , Brigitte Bressac-De, Bronner , Myriam, Buell , Crystal M., Collod-Béroud , Gwenaëlle, Coulet , Florence, Derive , Nicolas, Divincenzo , Christina, Elzinga , Christopher D., Garrec , Celine, Houdayer , Claude, Karbassi , Izabela, Lizard , Sarab, Love , Angela, Muller , Danièle, Nagan , Narasimhan, Nery , Camille R., Rai , Ghadi, Révillion , Françoise, Salgado , David, Sevenet , Nicolas, Sinilnikova , Olga, Sobol , Hagay, Stoppa-Lyonnet , Dominique, Toulas , Christine, Trautman , Edwin, Vaur , Dominique, Vilquin , Paul, Weymouth , Katelyn S., Willis , Alecia, Eisenberg , Marcia, Strom , Charles M., Variant , Lab Corp Amer, Variant , Quest Diagnostics, Lab , UNICANCER Genetic Grp BRCA
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2016, 37 (12, SI), pp.1318-1328. 〈10.1002/humu.23113〉
Human Mutation, Wiley, 2016, 37 (12, SI), pp.1318-1328. 〈10.1002/humu.23113〉
International audience; As next-generation sequencing increases access to human genetic variation, the challenge of determining clinical significance of variants becomes ever more acute. Germline variants in the BRCA1 and BRCA2 genes can confer subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3379::e5f5f224d6252f42d9439c3bc93f1dd5
https://hal.archives-ouvertes.fr/hal-01469067
https://hal.archives-ouvertes.fr/hal-01469067
