What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant

Mijovic, Marija; Bukva, Bojan; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Cuturilo, Goran

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eNauka > Rezultati > What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant

Naziv:	What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variant
Autori:	Mijovic, Marija; Bukva, Bojan; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Cuturilo, Goran
Godina:	2022
Publikacija:	EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN:	1018-4813 European Journal of Human Genetics Pretraži identifikator
Tip rezultata:	Konferencijski rad
Kolacija:	vol. 30 br. SUPPL 1 str. 181-181
WoS-ID:	000779367700479
URI:	https://enauka.gov.rs/handle/123456789/816193
Izvor metapodataka:	(Preuzeto iz Nasi u WoS)
M-kategorija:	Mp kategorija će biti prikazana naknadno.

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