| Literature DB >> 2714786 |
Abstract
Clinical and cytogenetical findings are described in an infant with a de novo deletion of the long arm of chromosome 2. The boy's karyotype is 46,XY, rec(2)delq,t(2;7) (2pter----2q34::7p21----7pter) (7qter----7p21::2q36----2qter). He showed developmental retardation, low-set ears, micrognathia, short, neck, abundant skin of the neck, tetralogy of Fallot, bipartite labialike scrotum, clitorislike penis, cryptorchism, and deformities of the hands and feet.Entities:
Mesh:
Year: 1989 PMID: 2714786 DOI: 10.1007/BF00288283
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132