Showing 1 - 2 results of 2 for search 'Petra Loid', query time: 0.02s Refine Results
  1. 1
    GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children

    GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children by Petra Loid, Petra Loid, Petra Loid, Minna Pekkinen, Minna Pekkinen, Minna Pekkinen, Monica Reyes, Taina Mustila, Taina Mustila, Heli Viljakainen, Heli Viljakainen, Harald Jüppner, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie

    Published 2020
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  2. 2
    Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome

    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 2022
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