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Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious

Carla Bizzarri1, Francesca Crea, Romana Marini

  • 1Endocrinology Unit, Bambino Gesú Children's Hospital, IRCCS, P.zza S. Onofrio 4 00165, Rome, Italy. carla.bizzarri@opb.net

Journal of Pediatric Endocrinology & Metabolism : JPEM
|January 19, 2013
PubMed

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