A Cross-sectional Study on Molecular Cartography: The Mapping of Down Syndrome with Cytogenetic Tools

Introduction: Down Syndrome (DS), or trisomy 21, is the most common genetic cause of intellectual disability among children, with an incidence of 1 in 700 births. This extra copy of chromosome 21 leads to characteristic clinical features known as Down facies, which include microcephaly, hyperteloris...

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Bibliographic Details
Main Authors: A Deepa, K Chandramouleeswari, M Dougul Regis
Format: Article
Language:English
Published: JCDR Research and Publications Pvt. Ltd. 2025-01-01
Series:National Journal of Laboratory Medicine
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Online Access:https://www.njlm.net/articles/PDF/2896/74501_CE[Ra1]_F(SHU)_QC(AN_SHU)_PF1(VD_SHU)_redo_PFA(SHU)_PB(VD_SHU)_PN(SHU).pdf
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