Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hana Dynkova Filkova"'
Autor:
Marketa Wayhelova, Vladimira Vallova, Petr Broz, Aneta Mikulasova, Jan Smetana, Hana Dynkova Filkova, Dominika Machackova, Kristina Handzusova, Renata Gaillyova, Petr Kuglik
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Neurodevelopmental disorders (NDDs) and/or associated multiple congenital abnormalities (MCAs) represent a genetically heterogeneous group of conditions with an adverse prognosis for the quality of intellectual and social abilitie
Externí odkaz:
https://doaj.org/article/46268ac87d8b4810be2aceadfdb01208
Autor:
Wayhelova, Marketa1,2 (AUTHOR) marketa.wayhelova@mail.muni.cz, Vallova, Vladimira1,2 (AUTHOR), Broz, Petr1,3 (AUTHOR), Mikulasova, Aneta4 (AUTHOR), Smetana, Jan1 (AUTHOR), Dynkova Filkova, Hana2 (AUTHOR), Machackova, Dominika1 (AUTHOR), Handzusova, Kristina1 (AUTHOR), Gaillyova, Renata5 (AUTHOR), Kuglik, Petr1,2 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 2/6/2024, Vol. 19 Issue 1, p1-12. 12p.
Autor:
Wayhelova, Marketa1,2 (AUTHOR) marketa.wayhelova@mail.muni.cz, Vallova, Vladimira1,2 (AUTHOR), Broz, Petr1,3 (AUTHOR), Mikulasova, Aneta4 (AUTHOR), Machackova, Dominika1 (AUTHOR), Filkova, Hana Dynkova2 (AUTHOR), Smetana, Jan1 (AUTHOR), Takacsova, Alena5 (AUTHOR), Gaillyova, Renata5 (AUTHOR), Kuglik, Petr1,2 (AUTHOR) marketa.wayhelova@mail.muni.cz
Publikováno v:
Molecular Medicine Reports. May2023, Vol. 27 Issue 5, pN.PAG-N.PAG. 1p.