Article
Clinical phenotype associated with terminal 2q37 deletion.
Clinical genetics - 1 Sept 1995
Conrad B, Dewald G, Christensen E, Lopez M, Higgins J, Pierpont M E
Abstract excerpt
Three children with deletions of the terminal portion of the long arm of chromosome 2 [del (2) (q37)] are described and their clinical findings compared to published cases of 2q terminal deletions. Common clinical findings include development delay, macrocephaly, frontal bossing, depressed nasal...
Topics
- Abnormalities, Multiple
- Chromosome Deletion
- Chromosomes, Human, Pair 2
- Humans
- Infant
- Karyotyping
- Male
- Phenotype