9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition

Am J Med Genet A. 2016 Apr;170A(4):1095-8. doi: 10.1002/ajmg.a.37534. Epub 2016 Jan 5.

Authors

Megan Crone¹, Mary Ann Thomas^{2

3}

Affiliations

¹ Section of Pediatrics, Department of Neurology, Cumming School of Medicine, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.
² Department of Medical Genetics, Cumming School of Medicine, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.
³ Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Alberta, Canada.

PMID: 26728902
DOI: 10.1002/ajmg.a.37534

No abstract available

Publication types

Case Reports

MeSH terms

Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Comparative Genomic Hybridization
Echocardiography
Electrocardiography
Facies
Female
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Phenotype
Rare Diseases / diagnosis
Rare Diseases / genetics