TY  - GEN
AU  - Hernández-Porras, Isabel
AU  - Jiménez-Catalán, Beatriz
AU  - Schuhmacher, Alberto J
AU  - Guerra, Carmen
PY  - 2015
DO  - 10.1080/21675511.2015.1045169
SN  - 2167-5511
UR  - http://hdl.handle.net/20.500.12105/19851
AB  - Noonan syndrome (NS) is an autosomal dominant genetic disorder characterized by short stature, craniofacial dysmorphism, and congenital heart defects. A significant fraction of NS-patients also develop myeloproliferative disorders. The penetrance of...
LA  - eng
PB  - Taylor & Francis
TI  - The impact of the genetic background in the Noonan syndrome phenotype induced by K-Ras(V14I).
TY  - research article
ER  -