Perspectives on the application of cytogenomic approaches in chronic lymphocytic leukaemia
WN Wan Mohamad Zamri, N Mohd Yunus… - Diagnostics, 2023 - mdpi.com
Chronic lymphocytic leukaemia (CLL) is a haematological malignancy characterised by the
accumulation of monoclonal mature B lymphocytes (positive for CD5+ and CD23+) in …
accumulation of monoclonal mature B lymphocytes (positive for CD5+ and CD23+) in …
[HTML][HTML] Navigating the non-coding genome in heart development and Congenital Heart Disease
Abstract Congenital Heart Disease (CHD) is characterised by a wide range of cardiac
defects, from mild to life-threatening, which occur in babies worldwide. To date, there is no …
defects, from mild to life-threatening, which occur in babies worldwide. To date, there is no …
Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
W Bai, Q Zhang, Z Lin, J Ye, X Shen, L Zhou… - Frontiers in …, 2023 - frontiersin.org
Introduction Embryonic chromosomal abnormalities represent a major causative factor in
early pregnancy loss, highlighting the importance of understanding their role in spontaneous …
early pregnancy loss, highlighting the importance of understanding their role in spontaneous …
Sequencing: A Promising Path in the Detection of Fetal Health
I Sharma, N Negi, SC Saha - Non-invasive Prenatal Screening (NIPS) in …, 2024 - Springer
Sequencing technology enables prenatal screening by noninvasive detection of fetal health
through cell-free fetal DNA in the mother's circulation. This approach offers early diagnosis …
through cell-free fetal DNA in the mother's circulation. This approach offers early diagnosis …
[HTML][HTML] Cytogenomic Microarray Testing
Cytogenomic microarray testing allows the detection of submicroscopic genomic
rearrangements, commonly denominated copy number variations (CNVs) that are implicated …
rearrangements, commonly denominated copy number variations (CNVs) that are implicated …
Caractérisation de variants génétiques de vulnérabilité à l'épilepsie chez des familles Algériennes
A Chentouf - 2016 - theses.hal.science
L'existence d'une composante génétique dans l'épilepsie est connue depuis des années
grâce aux études épidémiologiques de concordance entre jumeaux et d'agrégation …
grâce aux études épidémiologiques de concordance entre jumeaux et d'agrégation …
[PDF][PDF] PRUEBAS DE DIAGNÓSTICO Y CRIBADO GENÉTICO
NEF CASTRO - repository.urosario.edu.co
El diagnóstico de una patología de origen genético es útil para identificar el origen de la
enfermedad, en algunos casos sirve para establecer el pronóstico o el tratamiento del …
enfermedad, en algunos casos sirve para establecer el pronóstico o el tratamiento del …
Cytogenomic Microarray Testing
Cytogenomic microarray testing allows the detection of submicroscopic genomic
rearrangements, commonly denominated copy number variations (CNVs) that are implicated …
rearrangements, commonly denominated copy number variations (CNVs) that are implicated …
КРАТКИЙ ОБЗОР ВОЗМОЖНОСТЕЙ ХРОМОСОМНОГО МИКРОМАТРИЧНОГО АНАЛИЗА В ПРЕНАТАЛЬНОЙ ДИАГНОСТИКЕ
АВ Барсуков, ИВ Горпинич - … ТРАНСЛЯЦИОННАЯ МЕДИЦИНА. ОПЫТ …, 2019 - elibrary.ru
В обзоре рассмотрены возможности применения хромосомного микроматричного
анализа в качестве неинвазивного метода пренатальной диагностики. Кратко описаны …
анализа в качестве неинвазивного метода пренатальной диагностики. Кратко описаны …