Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia

Subjects

Subjects :

Genetics
Comparative Genomic Hybridization
Pediatrics
medicine.medical_specialty
business.industry
Cancer
DNA
medicine.disease
Pancytopenia
Chromosome Banding
Developmental disorder
Intellectual Disability
Karyotyping
Myelodysplastic Syndromes
medicine
Humans
Abnormalities, Multiple
Female
Chromosomes, Human, Pair 3
Chromosome Deletion
Child
business
In Situ Hybridization, Fluorescence
Genetics (clinical)

Details

ISSN :

15524833 and 15524825

Database :

OpenAIRE

Journal :

American Journal of Medical Genetics Part A

Accession number :

edsair.doi.dedup.....8a4e82d060fe34de93dfe42575dc3c55

Full Text :

https://doi.org/10.1002/ajmg.a.32857