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Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome
Lisenka E. L. M. Vissers, Monica Bonetti, Jeroen Paardekooper Overman, Willy M. Nillesen, Suzanna G. M. Frints, Joep de Ligt, Giuseppe Zampino, Ana Justino, Jose C. Machado, Marga Schepens, Han G. Brunner, Joris A. Veltman, Hans Scheffer, Piet Gros, Jose L. Costa, Marco Tartaglia, Ineke van der Burgt, Helger G. Yntema*, Jeroen den Hertog
*Corresponding author for this work
Research output: Contribution to journal › Article › Academic › peer-review