Phenotypic delineation of a 12q21 deletion syndrome
Clin Dysmorphol
.
2019 Oct;28(4):198-201.
doi: 10.1097/MCD.0000000000000274.
Authors
Caoimhe S McKenna
1
,
Nivedita Saxena
2
,
Tabib A Dabir
1
,
June Jones
1
,
Geoff Smith
1
,
Patrick J Morrison
1
3
Affiliations
1
Department of Genetic Medicine, Belfast City Hospital.
2
Department of Paediatrics, Ulster Hospital Dundonald.
3
Department of Clinical Genetics, Queens University Belfast, Belfast, UK.
PMID:
30985307
DOI:
10.1097/MCD.0000000000000274
No abstract available
Publication types
Case Reports
MeSH terms
Alleles
Chromosome Deletion*
Chromosome Disorders / diagnosis*
Chromosome Disorders / genetics*
Chromosomes, Human, Pair 12*
Comparative Genomic Hybridization
Genetic Markers
Humans
Infant
Male
Phenotype*
Syndrome
Substances
Genetic Markers