A novel atypical 22q11.2 distal deletion in father and son
J Med Genet
.
2002 Oct;39(10):E62.
doi: 10.1136/jmg.39.10.e62.
Authors
S Garcia-Miñaur
,
J Fantes
,
R S Murray
,
M E M Porteous
,
L Strain
,
J E Burns
,
J Stephen
,
J P Warner
PMID:
12362044
PMCID:
PMC1734988
DOI:
10.1136/jmg.39.10.e62
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adult
Chromosome Banding
Chromosome Deletion*
Chromosomes, Human, Pair 22 / genetics*
Craniofacial Abnormalities / genetics
Humans
Infant
Karyotyping
Male
Nuclear Family
Syndrome
Tetralogy of Fallot / genetics