Partial monosomy of chromosome 21 and congenital malformations monosomy of chromosome 21 and malformations

Clin Dysmorphol. 2020 Jul;29(3):165-166. doi: 10.1097/MCD.0000000000000310.

Authors

Lucas Osiak¹, João G Saraiva¹, Viviane de F Mestre¹, Lígia S L Ferrari², Wagner J M Paiva³, Renata L L F de Lima⁴, Maria J S Salles¹

Affiliations

¹ Laboratory of Developmental Toxicology, Department of General Biology, State University of Londrina.
² Department of Pediatrics and Pediatric Surgery, State University of Londrina.
³ Genetic Counseling Service, Department of General Biology, State University of Londrina, Londrina, Paraná.
⁴ Human Genetics and Mutagenesis Laboratory, Department of Genetics, Institute of Biology, Federal University of Bahia, Salvador, Brazil.

PMID: 32501867
DOI: 10.1097/MCD.0000000000000310

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 21 / genetics
Female
Humans
Infant
Monosomy / genetics*

Supplementary concepts

Chromosome 21 monosomy