Претрага
Резултати
A rare association of interrupted aortic arch type C and microdeletion 22q11.2
[2008]
Cuturilo, Goran; Drakulić, Danijela Routine jejunal endoscopic biopsy in children
[1996]
Vukavić Tamara Controversies in the RRT management [2016]
Stojanovic, Vesna DSocial-economic factors and irrational antibiotic use as reasons for antibiotic resistance of bacteria causing common childhood infections in primary healthcare [2011]
Ilić, Katarina; Jakovljević, Emil; Škodrić Trifunović, VesnaMicrobiological aspects of vulvovaginitis in prepubertal girls
[2012]
Ranđelović, Gordana 4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome [2011]
Čuturilo, GoranPrimary Budd-Chiari syndrome in a 3-year-old boy with homozygous factor V Leiden G1691A mutation [2014]
Boskovic, Aleksandra; Kitic, Ivana; Stankovic, Ivica; Prokic, Dragan; Zlatar, NadaThree siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation [2008]
Milenković, Tatjana; Koehler, Katrin; Krumbholz, Manuela; Živanović, Slađana; Zdravković, Dragan S.; Huebner, AngelaManifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature [2000]
Boerkoel, Cornelius F; O'Neill, S; Andre, Jean-Luc; Benke, PJ; Bogdanovic, Radovan M; Bulla, M; Burguet, A; Cockfield, Sandra; Cordeiro, Isabel; Ehrich, Jochen HH;
Frund, S; Geary, DF; Ieshima, A; Illies, F; Joseph, MW; Kaitila, I; Lama, Guiliana; Leheup, B; Ludman, MD; McLeod, DR; Medeira, A; Milford, David V; Ormala, T; Rener-Primec, Z; Santava, A; Santos, HG; Schmidt, Beate; Smith, Graham C; Spranger, J; Zupancic, N; Weksberg, R;
Genotype phenotype correlation in a pediatric population with antithrombin deficiency
[2019]
Kovač, Mirjana Филтери
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