Ara
Toplam kayıt 2, listelenen: 1-2
First observation of hemoglobin G-waimanalo and hemoglobin fontainebleau cases in the Turkish population
(Turkish Society of Hematology, 2016)
[No abstract available]
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
(Nature Publishing Group, 2016)
Purpose:Noonan syndrome (NS) is an autosomal-dominant disorder characterized by craniofacial dysmorphism, growth retardation, cardiac abnormalities, and learning difficulties. It belongs to the RASopathies, which are caused ...