Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
Title
Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
Identifier
/unibl/sci/idNaucniRad:22945
Type
See all items with this valueAcademic Article
Date
Bibliographic Citation
N. Marić, G. Bukara-Radujković, Lj. Solomun, D. Jojić, Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate, Central European Journal of Paediatrics, Vol. 14, No. 1, pp. 88 - 91, 2018
page start
88
page end
91
Is Part Of
See all items with this valueCentral European Journal of Paediatrics
See all items with this value2490-3671
list of authors
Relation
Position: 12514 (34 views)