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Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
Download from www.nature.comNeurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes
UploadNeuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients
Download from www.nature.comMutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
Download from www.researchgate.netCharacteristics and outcome of Goodpasture’s disease in children
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