Showing 1 - 3 results of 3 for search 'Tiina H. Ojala', query time: 0.03s Refine Results
  1. 1
    Renal‐hepatic‐pancreatic dysplasia type 2: Perinatal lethal condition or a multisystemic disorder with variable expressivity

    Renal‐hepatic‐pancreatic dysplasia type 2: Perinatal lethal condition or a multisystemic disorder with variable expressivity by Kathryn Gunther, Essam M. Imseis, Joyce P. Samuel, Elizabeth A. Hillman, Tiina H. Ojala, Timo Jahnukainen, Paul R. Hillman

    Published 2023-04-01
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  2. 2
    Recessive TMOD1 mutation causes childhood cardiomyopathy

    Recessive TMOD1 mutation causes childhood cardiomyopathy by Catalina Vasilescu, Mert Colpan, Tiina H. Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Laura Martelius, Reena Kumari, Helena Hinterding, Virginia Brilhante, Simo Ojanen, Pekka Lappalainen, Juha Koskenvuo, Christopher J. Carroll, Velia M. Fowler, Carol C. Gregorio, Anu Suomalainen

    Published 2024-01-01
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    Article
  3. 3
    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy. by Juha W Koskenvuo, Inka Saarinen, Saija Ahonen, Johanna Tommiska, Sini Weckström, Eija H Seppälä, Sari Tuupanen, Tiia Kangas-Kontio, Jennifer Schleit, Krista Heliö, Julie Hathaway, Anders Gummesson, Pia Dahlberg, Tiina H Ojala, Ville Vepsäläinen, Ville Kytölä, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö

    Published 2021-01-01
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