Abstract:
:A female infant with total monosomy 21 identified by Q banding is described. The main clinical features were hypertonia, prominent occiput, hypertelorism, antimongoloid slant of the eyes, broad nose, "antimongoloid", character of dermatoglyphics. Both parents are phenotypically as well as karyotypically normal.
journal_name
Hum Genetjournal_title
Human geneticsauthors
Dziuba P,Dziekanowska D,Hübner Hdoi
10.1007/BF00270866subject
Has Abstractpub_date
1976-03-12 00:00:00pages
351-3issue
3eissn
0340-6717issn
1432-1203journal_volume
31pub_type
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