Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability
Clin Dysmorphol
.
2015 Oct;24(4):151-5.
doi: 10.1097/MCD.0000000000000096.
Authors
Rhoda S Akilapa
1
,
Kath Smith
,
Meena Balasubramanian
Affiliation
1
aSheffield Clinical Genetics Service bSheffield Diagnostic Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
PMID:
26267847
DOI:
10.1097/MCD.0000000000000096
No abstract available
Publication types
Case Reports
MeSH terms
Adult
Child
Chromosome Deletion*
Chromosomes, Human, Pair 12*
DNA Copy Number Variations
Genetic Association Studies
Humans
Intellectual Disability / genetics*
Male
Sequence Deletion