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Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome
- Authors :
- Hubrecht Institute with UMC
Cancer
Vissers, Lisenka E L M
Bonetti, Monica
Paardekooper Overman, Jeroen
Nillesen, Willy M.
Frints, Suzanna G M
De Ligt, Joep
Zampino, Giuseppe
Justino, Ana
Machado, José C.
Schepens, Marga
Brunner, Han G.
Veltman, Joris A.
Scheffer, Hans
Gros, Piet
Costa, José L.
Tartaglia, Marco
Van Der Burgt, Ineke
Yntema, Helger G.
Den Hertog, Jeroen
Hubrecht Institute with UMC
Cancer
Vissers, Lisenka E L M
Bonetti, Monica
Paardekooper Overman, Jeroen
Nillesen, Willy M.
Frints, Suzanna G M
De Ligt, Joep
Zampino, Giuseppe
Justino, Ana
Machado, José C.
Schepens, Marga
Brunner, Han G.
Veltman, Joris A.
Scheffer, Hans
Gros, Piet
Costa, José L.
Tartaglia, Marco
Van Der Burgt, Ineke
Yntema, Helger G.
Den Hertog, Jeroen
- Publication Year :
- 2015
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1395276808
- Document Type :
- Electronic Resource