| Literature DB >> 3314664 |
P Vanlieferinghen1, P Dechelotte, F Charbonné.
Abstract
A newborn with 10qter deletion is described and compared with the others previously reported cases. We confirm that the clinical features are not characteristic enough to delineate a syndrome in this chromosomal abnormality.Mesh：
Year: 1987 PMID： 3314664
Source DB: PubMed Journal: Ann Genet ISSN： 0003-3995