8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features

Clin Dysmorphol. 2020 Oct;29(4):207-209. doi: 10.1097/MCD.0000000000000338.

Authors

Jennifer T N LaBranche^{1

2}, Bob Argiropoulos^{1

3}, Mary Ann Thomas^{1

2}

Affiliations

¹ Departments of Medical Genetics.
² Pediatrics, University of Calgary.
³ Cytogenetics Laboratory, Alberta Public Laboratories, Calgary, Alberta, Canada.

PMID: 32740052
DOI: 10.1097/MCD.0000000000000338

No abstract available

Publication types

Case Reports

MeSH terms

Child
Chromosome Deletion*
Chromosome Disorders / diagnosis*
Chromosome Disorders / genetics*
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 8*
Comparative Genomic Hybridization
Facies
Genetic Association Studies*
Genetic Testing
Humans
Male
Phenotype*

Supplementary concepts

Chromosome 2, monosomy 2p22