Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?
Am J Med Genet
.
1997 Oct 3;72(1):111-4.
Authors
M G Butler
,
L K Hedges
,
P K Rogan
,
J R Seip
,
S B Cassidy
,
J B Moeschler
PMID:
9295086
PMCID:
PMC6025896
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child
Chromosomes, Human, Pair 15 / genetics*
Female
Humans
Klinefelter Syndrome / genetics*
Male
Prader-Willi Syndrome / genetics*
Trisomy / genetics*
X Chromosome*
Grants and funding
P01 HD030329/HD/NICHD NIH HHS/United States