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Ann Genet ; 20(4): 258-62, 1977 Dec.
Article in French | MEDLINE | ID: mdl-305753

ABSTRACT

A comparative study of five observations of a r (20) syndrome characterized by facial dysmorphism, the absence of severe malformations, and rather late onset of encephalopathy and seizures.


Subject(s)
Brain Diseases/genetics , Chromosome Aberrations , Chromosomes, Human, 19-20 , Face/abnormalities , Seizures/genetics , Brain Diseases/diagnosis , Child , Congenital Abnormalities/genetics , Female , Humans , Karyotyping , Seizures/diagnosis , Syndrome
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