Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Colobran, Roger"'
Autor:
Bosio, Mattia, Drechsel, Oliver, Rahman, Rubayte, Muyas, Francesc, Rabionet, Raquel, Bezdan, Daniela, Domenech Salgado, Laura, Hor, Hyun, Schott, Jean-Jacques, Munell, Francina, Colobran, Roger, Macaya, Alfons, Estivill, Xavier, Ossowski, Stephan
Mendelian diseases have shown to be an and efficient model for connecting genotypes to phenotypes and for elucidating the function of genes. Whole‐exome sequencing (WES) accelerated the study of rare Mendelian diseases in families, allowing for dir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1559::fbd92539e08bb90132f193c1820003b1
http://edoc.rki.de/176904/6312
http://edoc.rki.de/176904/6312
Autor:
Bosio, Mattia, Drechsel, Oliver, Rahman, Rubayte, Muyas, Francesc, Rabionet, Raquel, Bezdan, Daniela, Domenech Salgado, Laura, Hor, Hyun, Schott, Jean-Jacques, Munell, Francina, Colobran, Roger, Macaya, Alfons, Estivill, Xavier, Ossowski, Stephan
Mendelian diseases have shown to be an and efficient model for connecting genotypes to phenotypes and for elucidating the function of genes. Whole‐exome sequencing (WES) accelerated the study of rare Mendelian diseases in families, allowing for dir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ed18523bc6c02aaa4ee556702815153