Down Syndrome

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Down syndrome or trisomy 21 is caused by nondisjunction of chromosome 21 in a parent who is chromosomally normal and is one of the most common chromosomal abnormalities in liveborn children.

  1. REDIRECT trisomy 21
Retrieved from ‘https://embryology.med.unsw.edu.au/embryology/index.php?title=Down_Syndrome&oldid=1775’
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