Molecular Analysis Of The Additional X-Chromosome In Klinefelter's Syndrome Patients.
Indian J Hum Genet
;
1995 Jan; 1(1): 20-26
Article
Dans Anglais
| IMSEAR
| ID: sea-159753
ABSTRACT
The parental origin of the extra X chromosome in five families with Klinefelter's syndrome (47,XXY) was studied DNA restriction fragment length polymorphisms (RFLPs). In four, the extra X chromosome was maternal in origin and one it was paternal. Four X-linked marker loci were used and we were able to specify the origin of the extra X chromosome in all cases. The parental origin of the extra X chromosome in five families with Klinefelter's syndrome (47,XXY) was studied DNA restriction fragment length polymorphisms (RFLPs). In four, the extra X chromosome was maternal in origin and one it was paternal. Four X-linked marker loci were used and we were able to specify the origin of the extra X chromosome in all cases. The parental origin of the extra X chromosome in five families with Klinefelter's syndrome (47,XXY) was studied DNA restriction fragment length polymorphisms (RFLPs). In four, the extra X chromosome was maternal in origin and one it was paternal. Four X-linked marker loci were used and we were able to specify the origin of the extra X chromosome in all cases. The parental origin of the extra X chromosome in five families with Klinefelter's syndrome (47,XXY) was studied DNA restriction fragment length polymorphisms (RFLPs). In four, the extra X chromosome was maternal in origin and one it was paternal. Four X-linked marker loci were used and we were able to specify the origin of the extra X chromosome in all cases.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
langue:
Anglais
Texte intégral:
Indian J Hum Genet
Année:
1995
Type:
Article
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