An uncommon 3.4-Mb interstitial deletion at 3q29

Clin Dysmorphol. 2010 Jul;19(3):133-136. doi: 10.1097/MCD.0b013e3283387b21.

Authors

Jia-Chi Wang¹, Hetanshi Naik, Aneal Khan, Malgorzata J M Nowaczyk

Affiliation

¹ Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton Department of Pathology and Molecular Medicine Clinical Genetics Service, McMaster University Medical Centre, Hamilton, Ontario Alberta Children's Hospital, Shaganappi Trail, Calgary Department of Medical Genetics, University of Calgary, Alberta, Canada.

PMID: 20414105
DOI: 10.1097/MCD.0b013e3283387b21

No abstract available

Publication types

Case Reports

MeSH terms

Adolescent
Base Pairing / genetics*
Child
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 3 / genetics*
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Male
Pregnancy