| Literature DB >> 974255 |
A Khajavi, R S Lachman, D L Rimoin, R N Schimke, J P Dorst, A J Ebbin, S Handmaker, G Perreault.
Abstract
There appears to be definite heterogeneity within the campomelic syndromes. We are broadly classifying these into the classic or long bone campomelic syndromes and 2 distinct short bone varieties designated as the normocephalic short-boned and craniosynostotic short-boned types, respectively (Table 1).Mesh：
Year: 1976 PMID： 974255
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN： 0547-6844