Showing 1–9 of 9 results
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Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome
- Lisenka ELM Vissers
- , Monica Bonetti
- , Jeroen Paardekooper Overman
- , Willy M Nillesen
- , Suzanna G M Frints
- , Joep de Ligt
- , Giuseppe Zampino
- , Ana Justino
- , José C Machado
- , Marga Schepens
- , Han G Brunner
- , Joris A Veltman
- , Hans Scheffer
- , Piet Gros
- , José L Costa
- , Marco Tartaglia
- , Ineke van der Burgt
- , Helger G Yntema
- & Jeroen den Hertog
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