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PMID: 671488 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism.

Journal of medical genetics ·Vol. 15 ·No. 3 ·1978-06-00 ·Pages 222-6

Hsu LY, Paciuc S, David K, Cristian S, Moloshok R, Hirschhorn K

Abstract

暂无摘要

MeSH Terms
Azure Stains Chromosome Aberrations Female Humans Karyotyping Mosaicism Quinacrine Sex Chromosomes/ultrastructure Turner Syndrome/genetics X Chromosome/ultrastructure
Chemicals
Azure Stains Quinacrine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hsu L Y
Paciuc S
David K
Cristian S
Moloshok R
Hirschhorn K
References (12)
12 references, click to expand
  1. KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
    J Med Genet. 1965 Jun;2(2):142-55 PMID: 14295659
  2. Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter).
    Hum Genet. 1977 Nov 10;39(2):147-55 PMID: 598825
  3. Dicentric X isochromosomes in man.
    J Med Genet. 1976 Dec;13(6):496-500 PMID: 1018308
  4. Chromosomal and clinical findings in 110 females with Turner syndrome.
    Hum Genet. 1976 Dec 29;35(1):35-49 PMID: 1002163
  5. Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography.
    Stain Technol. 1972 Mar;47(2):87-93 PMID: 4113107
  6. A rapid banding technique for human chromosomes.
    Lancet. 1971 Oct 30;2(7731):971-2 PMID: 4107917
  7. Dicentric human X chromosomes.
    Hereditas. 1974;76(2):259-68 PMID: 4135824
  8. C bands in human metaphase chromosomes treated by barium hydroxide.
    Ann Genet. 1974 Jun;17(2):135-6 PMID: 4139928
  9. Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).
    Clin Genet. 1975 Apr;7(4):299-303 PMID: 47795
  10. Differences in human X isochromosomes.
    J Med Genet. 1975 Dec;12(4):378-89 PMID: 1219118
  11. Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15 q21)] in a patient with gonadal dysgenesis.
    Clin Genet. 1975 Jul;8(1):11-7 PMID: 1149316
  12. Isochromosome-X in man. I.
    Hereditas. 1966;54(3):260-76 PMID: 6001835
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.15.3.222
Published
1978-06-00
Pages
222-6
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1013682
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.15.3.222 PMC Full Text View journal details
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