Add to ORKGContains fulltext : 187340.pdf (publisher's version ) (Open Access)Radboud University, 20 april 2018Promotores : Noordam, C., Nijhuis-van der Sanden, M.W.G. Co-promotores : Draaisma, J.M.T., Burgt, C.J.A.M. van der195 p
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Contains fulltext : 202963.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 196861.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 147092.pdf (Publisher’s version ) (Open Access)128 p
Contains fulltext : 101058.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 56151.pdf (publisher's version ) (Closed access)1 p
Contains fulltext : 55786.pdf (publisher's version ) (Closed access)Although Noona...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Contains fulltext : 71196.pdf (publisher's version ) (Closed access)Although Noona...
Nous avons réalisé l'étude clinique détaillée de 51 patients, âgés de 1 à 57 ans, suivis dans l'Unit...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous devel...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Contains fulltext : 202963.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 196861.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 147092.pdf (Publisher’s version ) (Open Access)128 p
Contains fulltext : 101058.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 56151.pdf (publisher's version ) (Closed access)1 p
Contains fulltext : 55786.pdf (publisher's version ) (Closed access)Although Noona...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Contains fulltext : 71196.pdf (publisher's version ) (Closed access)Although Noona...
Nous avons réalisé l'étude clinique détaillée de 51 patients, âgés de 1 à 57 ans, suivis dans l'Unit...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous devel...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Background: Noonan syndrome spectrum disorders are a group of disorders caused by mutations in sever...