Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/1720
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dc.contributor.authorU.A. Jo`rayeva, F.A. Atakhodjaeva-
dc.date.accessioned2025-05-27T15:35:57Z-
dc.date.available2025-05-27T15:35:57Z-
dc.date.issued2025-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/1720-
dc.description.abstractAccording to the World Health Organization (WHO), 1 in every 700-100 children born has a genetic disorder, such as chromosomal abnormalities, including Down syndrome. Birth defects include structural abnormalities and genetic abnormalities in the fetus. Chromosome G-band karyotyping analysis is widely used as a method for detecting genetic abnormalities in clinical prenatal diagnosis. However, this approach has several limitations, including the necessity of performing cell culture, a lengthy detection wait period (2 to 3 weeks), and a low resolution (only chromosomal abnormalities > 5–10 Mb can be detected using this approach)en_US
dc.language.isoen_USen_US
dc.publisherO'zbekiston, Termizen_US
dc.titleEVALUATION OF MODERN DIAGNOSTIC METHODS FOR CHROMOSOMAL DISORDERS IN EARLY PREGNANCYen_US
dc.typeThesisen_US
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