Jojić, Dragica, Clinic for Children’s Diseases, University Clinical Centre of the Republic of Srpska, Bosnia and Herzegovina

• Vol 14, No 1 (2018): Central European Journal of Paediatrics - Case Report
  Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
  Abstract  PDF

The full text of articles published in this journal can be used free of charge for personal and educational purposes while respecting authors and publishers' copyrights. For commercial purposes no part of this journal may be reproduced without the written permission of the publisher.