Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
Naslov
Terminal deletion of chromosome 10p13 as a cause of hypoparathyroidism in a neonate
Identifikator
/unibl/sci/idNaucniRad:22945
Tip
Pronađite slične unoseAcademic Article
Datum
Bibliografski citat
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
Početna stranica
88
Krajnja stranica
91
Je dio
Central European Journal of Paediatrics
2490-3671
Lista autora
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