A rare case of a de novo dup(19q) associated with a mild phenotype
J Med Genet
.
2002 Oct;39(10):E61.
doi: 10.1136/jmg.39.10.e61.
Authors
M Qorri
,
P Oei
,
H Dockery
,
J McGaughran
PMID:
12362043
PMCID:
PMC1734984
DOI:
10.1136/jmg.39.10.e61
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Chromosomes, Human, Pair 19 / genetics*
Developmental Disabilities / genetics
Female
Gene Duplication*
Humans
Phenotype