Abstract
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.
Publication types
-
Case Reports
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Chromosome Deletion*
-
Chromosome Mapping
-
Chromosomes, Human, Pair 6*
-
DNA Probes
-
Facial Bones / abnormalities*
-
Humans
-
Infant, Newborn
-
Karyotyping
-
Male
-
Microcephaly / genetics*
-
Pedigree
-
Phenotype
-
Psychomotor Disorders / genetics*