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Ann Genet. 1988;31(4):247-9.

A case of monosomy 21.

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1
Institut za zdravstvenu zastitu majke i deteta Srbije, Laboratorija za citogenetiku, Novi Beograd, Yugosiavia.

Abstract

A new case of monosomy 21 was observed in a newborn male. Characteristic clinical features include: an antimongoloid eye slants, large and low set ears, flat nose bridge, hypoplastic nipples, cardiac anomalies, muscular hypotonia, retarded psychomotor development. The karyotypes of the parents were normal.

PMID:
3265310
[Indexed for MEDLINE]
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