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  1. Pasqualetti, Stefano [Editor]; Mattioni, Gloria [Editor] ; Edra

    Edra : our story

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    Milano: Skira, 2017

  2. Marbach, Felix [Author]; Stoyanov, Georgi [Author]; Erger, Florian [Author]; Stratakis, Constantine A. [Author]; Settas, Nikolaos [Author]; London, Edra [Author]; Rosenfeld, Jill A. [Author]; Torti, Erin [Author]; Haldeman-Englert, Chad [Author]; Sklirou, Evgenia [Author]; Kessler, Elena [Author]; Ceulemans, Sophia [Author]; Nelson, Stanley F. [Author]; Martinez-Agosto, Julian A. [Author]; Palmer, Christina G. S. [Author]; Signer, Rebecca H. [Author]; Andrews, Marisa V. [Author]; Grange, Dorothy K. [Author]; Willaert, Rebecca [Author]; Person, Richard [Author]; Telegrafi, Aida [Author]; Sievers, Aaron [Author]; Laugsch, Magdalena [Author]; Theiß, Susanne [Author]; [...]

    Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

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    08 April 2021

    Published in: Genetics in medicine ; 23(2021), 8, Seite 1465-1473