RT Journal Article
SR Electronic
T1 Del(4)(q33----qter): another case report of a child with mild dysmorphism.
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP 776
OP 778
DO 10.1136/jmg.26.12.776
VO 26
IS 12
A1 Fagan, K A
A1 Morris, R B
YR 1989
UL http://jmg.bmj.com/content/26/12/776.abstract
AB A male child is described with some growth and developmental delay and other minor dysmorphic features. Chromosome analysis showed a de novo deletion of the q33----qter terminal segment of a chromosome 4. There has been published discussion concerning the severity of phenotypic malformations in the seven cases described so far with this particular deletion. We add details of our patient to help to delineate further features of this syndrome.