A novel presentation of a rare chromosome 2p25.2 deletion
Clin Dysmorphol
.
2010 Apr;19(2):101-102.
doi: 10.1097/MCD.0b013e328337bb28.
Authors
Kristin Becker
1
,
Charlotte Jaggard
,
Sarah Horrocks
Affiliation
1
North Wales Clinical Genetics Service, Glan Clwyd Hospital Department of Community Paediatrics, Royal Alexandra Hospital, Rhyl Institute of Medical Genetics, University Hospital of Wales, Cardiff, UK.
PMID:
20173628
DOI:
10.1097/MCD.0b013e328337bb28
No abstract available
Publication types
Case Reports
MeSH terms
Child
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 2 / genetics*
Female
Humans
Infant
Infant, Newborn
Male
Pregnancy