Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome

Clin Dysmorphol. 2010 Jul;19(3):137-139. doi: 10.1097/MCD.0b013e328338807d.

Authors

Charlotte W Ockeloen¹, Nicole de Leeuw, Hanneke Mieloo, Ineke G M Reijnen, Bert B A de Vries

Affiliation

¹ Department of Human Genetics, Radboud University, Nijmegen Medical Centre, Nijmegen Department of Pediatrics, St Elisabeth Medical Centre, Tilburg, The Netherlands.

PMID: 20357662
DOI: 10.1097/MCD.0b013e328338807d

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Abnormalities, Multiple / genetics*
Child
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 22 / genetics*
Chromosomes, Human, Pair 8 / genetics*
Female
Humans
Infant
Infant, Newborn
Phenotype
Pregnancy
Syndrome