Chery M, Formiga L F, Mujica P, André M, Stehelin D, Dozier C, Gilgenkrantz S
Laboratoire de Génétique, Centre Régional de Transfusion Sanguine de Nancy-Brabois, Van Doeuvre-Les-Nancy.
Ann Genet. 1989;32(2):82-6.
A de novo interstitial deletion of 6q21 was observed in a male baby with moderate microcephaly, facial dysmorphism, and psychomotor retardation. In situ hybridization with a c-myb probe showed that the gene was conserved on the deleted chromosome.