Butler L J, Palmer A V, Spencer T, Tabios-Broadway R, Wall W J
Clin Genet. 1987 Apr;31(4):199-205. doi: 10.1111/j.1399-0004.1987.tb02796.x.
A female child is described with multiple anomalies including epicanthus, frontal bossing, short sternum, polydactyly, cleft of the larynx, renal cysts, and unusual dermatoglyphics. She died aged 3 months and was found to have a unique de novo deletion of chromosome No. 4 (q22-q25). This case is compared with other long arm deletions of 4q and reference made to assignment of genetic markers to chromosome No. 4.