Hannele Koillinen

- Docent,
Institute of Biomedicine (Faculty of Medicine)

hakoil@utu.fi

Publications

Älyllisen kehitysvammaisuuden genetiikka - etiologia ja etiologian selvittely (2023)
- Duodecim
Koillinen Hannele, Arvio Maria
(D1 Article in a professional journal)
Kolmas sektori on tuki kliinikoille harvinaissairauksissa (2023)
- Lääkärilehti
Heikkinen Risto, Laine Merja K., Koillinen Hannele, Salmi Satu, Rantanen Elina
(A2 Refereed review article in a scientific journal )
PHIP-associated Chung-Jansen syndrome: Report of 23 new individuals (2023)
- Frontiers in cell and developmental biology
Kampmeier Antje, Leitão Elsa, Parenti Ilaria, Beygo Jasmin, Depienne Christel, Bramswig Nuria C, Hsieh Tzung-Chien, Afenjar Alexandra, Beck-Wödl Stefanie, Grasshoff Ute, Haack Tobias B, Bijlsma Emilia K, Ruivenkamp Claudia, Lausberg Eva, Elbracht Miriam, Haanpää Maria K, Koillinen Hannele, Heinrich Uwe, Rost Imma, Jamra Rami Abou, Popp Denny, Koch-Hogrebe Margarete, Rostasy Kevin, López-González Vanessa, Sanchez-Soler Maria José, Macedo Catarina, Schmetz Ariane, Steinborn Carmen, Weidensee Sabine, Lesmann Hellen, Marbach Felix, Caro Pilar, Schaaf Christian P, Krawitz Peter, Wieczorek Dagmar, Kaiser Frank J, Kuechler Alma
(A1 Refereed original research article in a scientific journal)
Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Disease (2023)
- Pediatric and Developmental Pathology
Keskinen Sini, Paakkola Teija, Mattila Mirjami, Hietala Marja, Koillinen Hannele, Laine Jukka, Haanpää Maria K
(A1 Refereed original research article in a scientific journal)