Detection of a familial cryptic translocation by fluorescent in situ hybridisation.
AUTOR(ES)
Smith, D P
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1051821Documentos Relacionados
- Familial complex chromosome rearrangement ascertained by in situ hybridisation.
- Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.
- Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation.
- Detection of Campylobacter pylori in stomach tissue by DNA in situ hybridisation.
- A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.