Clinical features associated with a 15.41 Mb deletion of chromosome 13q encompassing the MIR17HG locus

Clin Dysmorphol. 2013 Apr;22(2):68-70. doi: 10.1097/MCD.0b013e32835f56b3.

Authors

Hanis S Sharaidin¹, Stephen Knipe, Nicole Bain, Himanshu Goel

Affiliation

¹ University of Newcastle, Callaghan Department of Paediatrics, John Hunter Children's Hospital Molecular Cytogenetics, Department of Molecular Medicine, Hunter Area Pathology Service, John Hunter Hospital, New Lambton Heights Hunter Genetics, Waratah, New South Wales, Australia.

PMID: 23448905
DOI: 10.1097/MCD.0b013e32835f56b3

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / genetics
Abnormalities, Multiple / pathology*
Base Sequence
Chromosome Deletion*
Chromosomes, Human, Pair 13 / genetics*
Comparative Genomic Hybridization
Female
Genetic Loci
Humans
Infant
MicroRNAs / genetics*
Microcephaly / genetics
Microcephaly / pathology
Phenotype
RNA, Long Noncoding

Substances

MIR17HG, human
MicroRNAs
RNA, Long Noncoding