Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature

Clin Dysmorphol. 2019 Jan;28(1):53-56. doi: 10.1097/MCD.0000000000000245.

Authors

Neha S Bhatia¹, Jiin-Ying Lim¹, Maggie S Brett², Ene-Choo Tan^{2

3}, Hai Yang Law^{4

3}, Biju Thomas^{1

3}, Jonathan Choo^{5

3}, Angeline H M Lai^{1

3}, Saumya S Jamuar^{1

3}

Affiliations

¹ Department of Paediatrics.
² KK Research Centre.
³ Paediatric Academic Clinical Programme, SingHealth Duke-NUS Medical School, Singapore, Singapore.
⁴ DNA Diagnostic and Research Laboratory.
⁵ Department of Paediatric Subspecialties, KK Women's and Children's Hospital.

PMID: 30507726
DOI: 10.1097/MCD.0000000000000245

No abstract available

Publication types

Case Reports
Letter
Review

MeSH terms

Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 12 / genetics*
Female
Gene Deletion
Heart Defects, Congenital / genetics*
Humans
Infant
Male