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Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome.
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- المؤلفون: Vissers, Lisenka ELM1; Bonetti, Monica2; Paardekooper Overman, Jeroen2; Nillesen, Willy M3; Frints, Suzanna G M4; de Ligt, Joep1; Zampino, Giuseppe5; Justino, Ana6; Machado, José C6; Schepens, Marga3; Brunner, Han G1; Veltman, Joris A1; Scheffer, Hans3; Gros, Piet7; Costa, José L6; Tartaglia, Marco8; van der Burgt, Ineke3; Yntema, Helger G9; den Hertog, Jeroen10
- المصدر:
European Journal of Human Genetics. Mar2015, Vol. 23 Issue 3, p317-324. 8p.
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