Prenatal diagnosis of lissencephaly: A case report.

Autor: Cerovac, Nataša^1,2 mimanana@Eunet.rs, Terzić, Milan^2,3, Borković, Milan¹, Divac, Nevena^2,4, Stojanović, Radan^2,4, Prostran, Milica^2,4

Publikováno v: Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia. Jan2016, Vol. 73 Issue 1, p77-82. 6p. 2 Graphs.

PRENATALNA DIJAGNOZA VARIKSA INTRAABDOMINALNOG DELA UMBILIKALNE VENE - PRIKAZ SLUČAJA.

Autor: Novakov-Mikić, Aleksandra, Stojić, Siniša

Publikováno v: Medical Review / Medicinski Pregled. 2008, Vol. 61 Issue 1/2, p75-78. 4p. 2 Black and White Photographs.

Prenatalna dijagnoza daun sindroma – savremeni pristup

Autor: Maksić, Jasmina, Ninković, Dragan

Publikováno v: Zbornik radova-„Istraživanja u specijalnoj edukaciji i rehabilitaciji / Research in Special Education and Rehabilitation“,Beograd / Belgrade,2009

Daun sindrom (DS) ili trizomija hromozoma 21, je načešći oblik mentalne zaostalosti praćen specitičnim telesnim osobinama. Odavno je pokazana veza godina starosti majke i rađanja dece sa ovom trizomijom, pa je praksa da se invazivne dijagnosti�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10164::db0ffe521baf3b349e48715a2cf9debb
https://hdl.handle.net/21.15107/rcub_rfasper_4509

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The importance of direct genetic testing to determine female carriers in dystrophinopathies

Autor: Maksić, Jasmina, Maksimović, Nela, Rasulić, Lukas, Milankov, Olgica, Marjanović, Ana, Cvetković, Dragana, Rakočević, Vidosava, Rakočević Stojanović, Vidosava, Novaković, Ivana

Publikováno v: Vojnosanitetski pregled

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused by mutations in the dystrophin gene. They are X-linked recessive diseases, where males are affected and females are mostly healthy carriers of the mutation. It is estima

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10164::e37ef130c1c300328e99a0b5124bbf42
http://rfasper.fasper.bg.ac.rs/handle/123456789/4756