Familial deletions of chromosome 22q11: the Leuven experience
Am J Med Genet
.
1998 Dec 28;80(5):531-2.
Authors
A Swillen
,
K Devriendt
,
G Vantrappen
,
A Vogels
,
N Rommel
,
J P Fryns
,
B Eyskens
,
M Gewillig
,
M Dumoulin
PMID:
9880224
No abstract available
Publication types
Letter
Comment
MeSH terms
Belgium
Bias
Chromosome Deletion*
Chromosomes, Human, Pair 22 / genetics*
Female
Humans
Male
Phenotype