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High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results by Siggberg Linda, Sirpa Ala-Mello, Tarja Linnankivi, Kristiina Avela, Ilari Scheinin, Kati Kristiansson, Päivi Lahermo, Marja Hietala, Liisa Metsähonkala, Esa Kuusinen, Maarit Laaksonen, Janna Saarela, Sakari Knuutila
Published 2012Connect to this object online.
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Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome by Petra Loid, Petra Loid, Petra Loid, Marita Lipsanen-Nyman, Marita Lipsanen-Nyman, Sirpa Ala-Mello, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Juha Kere, Juha Kere, Juha Kere, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Mari Muurinen, Mari Muurinen, Mari Muurinen
Published 2022Connect to this object online.
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