Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Luciana Ribeiro"'
Autor:
Antonio Marcondes Lerario, Dipika R. Mohan, Luciana Ribeiro Montenegro, Mariana Ferreira de Assis Funari, Mirian Yumie Nishi, Amanda de Moraes Narcizo, Anna Flavia Figueredo Benedetti, Sueli Mieko Oba-Shinjo, Aurélio José Vitorino, Rogério Alexandre Scripnic Xavier dos Santos, Alexander Augusto de Lima Jorge, Luiz Fernando Onuchic, Suely Kazue Nagahashi Marie, Berenice Bilharinho Mendonca
Publikováno v:
Clinics, Vol 75 (2020)
OBJECTIVES: High-throughput sequencing of genomes, exomes, and disease-focused gene panels is becoming increasingly common for molecular diagnostics. However, identifying a single clinically relevant pathogenic variant among thousands of genetic poly
Externí odkaz:
https://doaj.org/article/a3a74911a39240788ce158a7327501af
Autor:
Amanda de Moraes Narcizo, Anna Flavia Figueredo Benedetti, Suely Kazue Nagahashi Marie, Dipika R. Mohan, Sueli Mieko Oba-Shinjo, Mirian Yumie Nishi, Aurélio José Vitorino, Alexander A. L. Jorge, Luciana Ribeiro Montenegro, Antonio M. Lerario, Rogério Alexandre Scripnic Xavier dos Santos, Berenice B. Mendonca, Luiz F. Onuchic, Mariana F A Funari
Publikováno v:
Clinics, Vol 75 (2020)
Clinics; v. 75 (2020); e1913
Clinics; Vol. 75 (2020); e1913
Clinics
Universidade de São Paulo (USP)
instacron:USP
Clinics, Volume: 75, Article number: e1913, Published: 10 AUG 2020
Clinics; v. 75 (2020); e1913
Clinics; Vol. 75 (2020); e1913
Clinics
Universidade de São Paulo (USP)
instacron:USP
Clinics, Volume: 75, Article number: e1913, Published: 10 AUG 2020
Objectives High-throughput sequencing of genomes, exomes, and disease-focused gene panels is becoming increasingly common for molecular diagnostics. However, identifying a single clinically relevant pathogenic variant among thousands of genetic polym
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.