Re-examining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study.
Sign Up to like & getrecommendations! Published in 2021 at "American journal of obstetrics and gynecology"
DOI: 10.1016/j.ajog.2021.03.050
Abstract: BACKGROUND The American College of Obstetricians and Gynecologists and the Society for Maternal Fetal Medicine recently recommended offering genetic counselling and diagnostic testing for enlarged NT at > 3.0mm, regardless of prior negative screening with… read more here.
Keywords: mom; atypical chromosome; diagnostic testing; chromosome abnormality ... See more keywords
Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality
Sign Up to like & getrecommendations! Published in 2022 at "Hematology"
DOI: 10.1080/16078454.2022.2071799
Abstract: ABSTRACT Introduction The aim of the study was to determine molecular genetic and clinical characterization of acute myeloid leukemia (AML) with trisomy 8 as the sole chromosome abnormality, a recurrent but rare chromosomal abnormality in… read more here.
Keywords: aml patients; trisomy sole; chromosome abnormality; sole chromosome ... See more keywords
Chromosome Abnormality Spectra and Clinical Impact in 1,787 Cases of Acute Leukemia in Koreans
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DOI: 10.1182/blood-2024-202685
Abstract: In acute leukemia, chromosomal alterations serve as diagnostic and prognostic markers, detectable via various techniques. Our institution previously studied chromosomal abnormalities over two periods of time, noting any differences. This study investigated the frequency of… read more here.
Keywords: chromosome abnormality; clinical impact; abnormality spectra; leukemia ... See more keywords