Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tommi Keski-Filppula"'
Autor:
Elisa Rahikkala, Johanna Julku, Sari Koskinen, Tommi Keski-Filppula, Sanna Häkli, Minna Kraatari-Tiri
Jones syndrome is a rare dominantly inherited syndrome characterized by gingival fibromatosis and progressive sensorineural hearing loss becoming symptomatic in the second decade of life. Here, we report a father and his two daughters presenting with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::153d5789004f8b502a75b4def255a09e
https://doi.org/10.21203/rs.3.rs-2007051/v1
https://doi.org/10.21203/rs.3.rs-2007051/v1
Autor:
Elisa Rahikkala, Johanna Julku, Sari Koskinen, Tommi Keski-Filppula, Stephanie Weissgraeber, Aida M. Bertoli-Avella, Sanna Häkli, Minna Kraatari-Tiri
Publikováno v:
European journal of human genetics : EJHG.
Jones syndrome is a rare dominantly inherited syndrome characterized by gingival fibromatosis and progressive sensorineural hearing loss becoming symptomatic in the second decade of life. Here, we report a father and his two daughters presenting with
Publikováno v:
Schizophrenia research. 216
Background Research-based evidence on patients with psychotic disorders involved in fatal motor vehicle accidents (FMVA) remains limited. The current study analyzes the characteristics of FMVA drivers, who had been hospitalized due to psychotic disor