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Ring chromosome 21 in a boy and a derivative chromosome 21 in the mother: Implication for ring chromosome formation

✍ Scribed by Muroya, Koji ;Yamamoto, Keiichi ;Fukushima, Yoshimitsu ;Ogata, Tsutomu


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
167 KB
Volume
110
Category
Article
ISSN
0148-7299

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## Abstract Ring chromosome 21 syndrome is a rare condition with a well‐characterized phenotype. Affected individuals have recognizable dysmorphic features, developmental delays, growth retardation, and a predisposition for congenital malformations involving the neurologic, craniofacial, digestive,