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Noonan Syndrome At a Glance

Noonan syndrome (NS) is caused by hyperactive SHP2 and is associated with cognitive deficits. Levy et al. find that. NMDA receptor (NMDAR)- ...






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FACT SHEET - CHILDCARE
Noonan syndrome is thought to occur in as many as between one in every 1000. The syndrome, a genetic disorder, has a number of features which vary in.
Noonan Syndrome Guideline Development Group
*Currently, mutation testing will prove a diagnosis of Noonan Syndrome in 70% of cases; in 30% the responsible gene remains unknown. The diagnosis of NS should ...
Open Praxis vol. 3 issue 1, March 2009
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