| WAYHELOVÁ, Markéta, Jan OPPELT, Jan SMETANA, Filip PARDY, Hana FILKOVÁ, Renata GAILLYOVÁ and Petr KUGLÍK. The clinical impact of targeted „next-generation“ sequencing in molecular diagnostics of intellectual disabilities and multiple congenital abnormalities. In The Biomania Student Scientific Meeting 2017. 2017. ISBN 978-80-210-8737-8. |
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@proceedings{1404610,
author = {Wayhelová, Markéta and Oppelt, Jan and Smetana, Jan and Pardy, Filip and Filková, Hana and Gaillyová, Renata and Kuglík, Petr},
booktitle = {The Biomania Student Scientific Meeting 2017},
language = {eng},
isbn = {978-80-210-8737-8},
title = {The clinical impact of targeted „next-generation“ sequencing in molecular diagnostics of intellectual disabilities and multiple congenital abnormalities},
year = {2017}
}
TY - CONF
ID - 1404610
AU - Wayhelová, Markéta - Oppelt, Jan - Smetana, Jan - Pardy, Filip - Filková, Hana - Gaillyová, Renata - Kuglík, Petr
PY - 2017
TI - The clinical impact of targeted „next-generation“ sequencing in molecular diagnostics of intellectual disabilities and multiple congenital abnormalities
SN - 9788021087378
ER -
WAYHELOVÁ, Markéta, Jan OPPELT, Jan SMETANA, Filip PARDY, Hana FILKOVÁ, Renata GAILLYOVÁ and Petr KUGLÍK. The clinical impact of targeted „next-generation“ sequencing in molecular diagnostics of intellectual disabilities and multiple congenital abnormalities. In \textit{The Biomania Student Scientific Meeting 2017}. 2017. ISBN~978-80-210-8737-8.
|
