Study on the relationship between cytogenetics and phenotypic effect in Turner’s syndrome
Hu Xiaofeng , Zhu Baosheng , Lin Hanhua , Shu Dan , Tao Deding , Wang Mudi
Current Medical Science ›› 1996, Vol. 16 ›› Issue (4) : 245 -248.
Study on the relationship between cytogenetics and phenotypic effect in Turner’s syndrome
The cytogenetics and clinical stigmata in 5 cases of Turner’s syndrome were studied. Three of them were non-mosaic i(Xq) and two with partial monosome of a X chromosome short are (Xp21). whose DNA replication patterns of inactive X chromosome were analyzed by RBG technique. Results showed that differences between the replication patterns in cases of X chromosome deletion (Xp21) and normal females existed; that the behavior of abnormal X expressed nonrandom inactivation. It was suggested that the phenotype may be closely related with both X chromosome replication pattern and its inactivation behavior, which might be useful in genetic counselling.
DNA replication / X chromosome / phenotypic effect / Turner’s syndrome
| [1] |
|
| [2] |
t(X:X)DNA 1988, 5(1): 15 |
| [3] |
|
| [4] |
ISCN. An international system for human cytogenetic nomenclature. Cytogenet Cell Genet, 1978, 21: 313-313 |
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
|
| [9] |
|
| [10] |
Midro A T, Kulikowski M, Sawicka A. Familial occurrence of isodicentric X chromosome with different breakpoints. Clin Genet, 1988: 34 |
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|
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