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Neuroblastoma expressed as catecholamine induced hypertrophic cardiomyopathy

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Fatal outcome of autosomal recessive polycystic kidney disease in neonates with recessive PKHD1 mutations

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신생아유전자스크리닝: 임상적, 유전학적 특징

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non-neurodegeneratiave etiology of walking difficulty in a boy with mucopolysaccharidosis type IIIC: bilateral femoral head necrosis

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