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A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features
Download from www.nature.comMetreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report
Download from doi.orgJapanese patient with Cole-carpenter syndrome with compound heterozygous variants of SEC24D
Download from api.wiley.comEndocrinological and phenotype evaluation in a patient with acrodysostosis
Download from doi.orgMeasles virus nucleocapsid protein increases osteoblast differentiation in Paget’s disease
Download from doi.orgCurrent concepts in perinatal mineral metabolism
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