Add to ORKGContains fulltext : 196861.pdf (publisher's version ) (Open Access)Radboud University, 20 november 2018Promotor : Noordam, C. Co-promotores : Draaisma, J.M.T., Burgt, C.J.A.M. van der124 p
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Contains fulltext : 182936.pdf (publisher's version ) (Closed access)Noonan syndro...
PURPOSE: To determine the full spectrum of ocular manifestations in patients with Noonan syndrome (N...
Contains fulltext : 187340.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 147092.pdf (Publisher’s version ) (Open Access)128 p
Item does not contain fulltextOBJECTIVE: This is the first cohort in which hearing impairment and ex...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
OBJECTIVE: This is the first cohort in which hearing impairment and external ear anomalies in Noonan...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
Contains fulltext : 193246.pdf (Publisher’s version ) (Open Access)The aim of this...
Os autores apresentam um caso de síndrome de Noonan em criança de 14 anos de idade, diagnosticada po...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Item does not contain fulltextPURPOSE: To determine the full spectrum of ocular manifestations in pa...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Contains fulltext : 182936.pdf (publisher's version ) (Closed access)Noonan syndro...
PURPOSE: To determine the full spectrum of ocular manifestations in patients with Noonan syndrome (N...
Contains fulltext : 187340.pdf (publisher's version ) (Open Access)Radboud Univers...
Contains fulltext : 147092.pdf (Publisher’s version ) (Open Access)128 p
Item does not contain fulltextOBJECTIVE: This is the first cohort in which hearing impairment and ex...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
OBJECTIVE: This is the first cohort in which hearing impairment and external ear anomalies in Noonan...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
Contains fulltext : 193246.pdf (Publisher’s version ) (Open Access)The aim of this...
Os autores apresentam um caso de síndrome de Noonan em criança de 14 anos de idade, diagnosticada po...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Item does not contain fulltextPURPOSE: To determine the full spectrum of ocular manifestations in pa...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Contains fulltext : 182936.pdf (publisher's version ) (Closed access)Noonan syndro...
PURPOSE: To determine the full spectrum of ocular manifestations in patients with Noonan syndrome (N...