Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter)
- PMID: 598825
- DOI: 10.1007/BF00287006
Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter)
Similar articles
-
[Human isodicentric X-chromosomes].Tsitologiia. 1977 Nov;19(11):1276-8. Tsitologiia. 1977. PMID: 601863 Russian.
-
Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations.J Med Genet. 1980 Dec;17(6):457-63. doi: 10.1136/jmg.17.6.457. J Med Genet. 1980. PMID: 7205428 Free PMC article.
-
Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic (Xq).Hum Genet. 1981;58(4):362-5. doi: 10.1007/BF00282816. Hum Genet. 1981. PMID: 7327558
-
Duplication of the short arm of the X chromosome in mother and daughter.Hum Genet. 1993 May;91(4):395-400. doi: 10.1007/BF00217366. Hum Genet. 1993. PMID: 8500796 Review.
-
[Genetic basis of Turner syndrome].Pol Arch Med Wewn. 1995 Oct;94(4):358-63. Pol Arch Med Wewn. 1995. PMID: 8834131 Review. Polish. No abstract available.
Cited by
-
The Turner phenotype and the different types of human x isochromosome.Hum Genet. 1981;57(2):159-64. doi: 10.1007/BF00282013. Hum Genet. 1981. PMID: 7228026 No abstract available.
-
DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics.Hum Genet. 1984;67(1):37-47. doi: 10.1007/BF00270556. Hum Genet. 1984. PMID: 6745924
-
Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476. Hum Genet. 1995. PMID: 7789944 Review.
-
Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism.J Med Genet. 1978 Jun;15(3):222-6. doi: 10.1136/jmg.15.3.222. J Med Genet. 1978. PMID: 671488 Free PMC article.
-
18Q - syndrome resulting from a tdic(14p; 18q).Hum Genet. 1979 Apr 17;48(1):61-6. doi: 10.1007/BF00273275. Hum Genet. 1979. PMID: 457135