Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Indian J Pediatr ; 2000 Nov; 67(11): 825-9
Article in English | IMSEAR | ID: sea-78727

ABSTRACT

Turner syndrome is a clinically defined phenotype that is characterized by partial or complete X chromosome monosomy. A host of cytogenetic aberrations and mosaicism have been associated with this syndrome. Some individuals, Turner syndrome variants, have cytogenetic findings consistent with Turner syndrome, but exhibit atypical clinical phenotypes. Recently, several molecular tests have been presented to allow for the refined clinical study of Turner syndrome and its variants.


Subject(s)
Cytogenetic Analysis/methods , Female , Humans , Mosaicism , Phenotype , Turner Syndrome/classification , X Chromosome/genetics , Y Chromosome/genetics
SELECTION OF CITATIONS
SEARCH DETAIL