| Literature DB >> 6431894 |
S Gilgenkrantz, A Morali, M Vidailhet, R Saura, F Serville, D Fontan, C Moraine.
Abstract
Three observations of r(14) are reported. Constant features of r(14) syndrome are the following: moderate but typical craniofacial dysmorphism, seizures and other neurological abnormalities, abnormal retinal pigmentation, and recurrent respiratory infections. The value of gene dosage evaluation for genes mapped to the distal segment of 14q, particularly the Ig heavy chain genes, is emphasized.Entities:
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Year: 1984 PMID: 6431894
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995