The Turkish Journal of Pediatrics
Smilar Issues: 6 Record Found
Congenital Hypothyroidism Screening Program in Turkey: A Local Evaluation
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Monitoring and Prognostic Evaluation of Patients with Congenital Hypothyroidism Treated in a Pediatric Endocrinology Unit
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Novel Nonsense Mutation of GPC3 Gene in a Patient with Simpson-Golabi-Behmel Syndrome
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Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism
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A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia
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Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years
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