Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes
K Boczkowski, Margareta Mikkelsen
Abstract
Open-access reader
K Boczkowski, Margareta Mikkelsen
Abstract
Open-access reader
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.
OpenAlex reports 40 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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.
Key concepts: Karyotype, Turner syndrome, Turner's syndrome, Chromosome, Fluorescence, X chromosome, Biology, Genetics