Deletion Xp22.3
J Med Genet
.
1990 Sep;27(9):598.
doi: 10.1136/jmg.27.9.598.
Authors
I K Temple
,
N R Dennis
PMID:
2231657
PMCID:
PMC1017228
DOI:
10.1136/jmg.27.9.598
No abstract available
Publication types
Letter
MeSH terms
Chromosome Deletion*
Female
Humans
Infant, Newborn
Sex Chromosome Aberrations / genetics*
Syndrome
X Chromosome*