Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes
AUTOR(ES)
Boczkowski, K.
RESUMO
Two patients with the clinical picture of Turner's syndrome showed a 46,XXp— and a 46,XXq— karyotype identified by a combination of fluorescence and autoradiography. Autoradiography showed that the abnormal X chromosome was indicated in most cells. The Xg findings in case 1 indicated that the abnormal X chromosome was of paternal origin.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1013055Documentos Relacionados
- Prevalence of cardiovascular malformations and association with karyotypes in Turner's syndrome.
- Turner's syndrome and 46,X,i(Yq) karyotype
- Bone demineralisation in patients with Turner's syndrome.
- Cytogenetic and molecular findings in patients with Turner's syndrome stigmata.
- Detection of Y mosaicism in patients with Turner's syndrome.