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Del (3) (p21.1-p13): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in a few reported cases. The manifestations linked to most genetic defects are often variable to some degree. More detailed information about the symptoms, causes, and treatments of Del (3) (p21.1-p13) is available below.
Read more about causes of Del (3) (p21.1-p13).
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