Home LiteratureArticle Details
PMID: 4475024 Published · ppublish English Journal Article

Abnormal X chromosomes in man: origin, behavior and effects.

Humangenetik ·Vol. 25 ·No. 1 ·1974-00-00 ·Pages 1-16

Therman E, Patau K

Abstract

暂无摘要

MeSH Terms
Amenorrhea/genetics Chromosome Aberrations Female Humans Male Phenotype Sex Chromatin Sex Chromosome Aberrations Sex Chromosomes Translocation, Genetic Trisomy Turner Syndrome
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Therman E
Patau K
References (46)
46 references, click to expand
  1. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].
    Ann Genet. 1970 Dec;13(4):245-8 PMID: 5313888
  2. [46, XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies].
    Humangenetik. 1973;20(2):163-6 PMID: 4785163
  3. A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C.
    Am J Hum Genet. 1965 Sep;17:377-83 PMID: 14334736
  4. Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).
    Proc Natl Acad Sci U S A. 1972 Jan;69(1):69-73 PMID: 4500556
  5. Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.
    Am J Hum Genet. 1971 Jul;23(4):410-8 PMID: 5097907
  6. Two human X-autosome translocations identified by autoradiography and fluorescence.
    Am J Hum Genet. 1972 Sep;24(5):583-97 PMID: 5054227
  7. Increased Q fluorescence of an inactive Xq-chromosome in man.
    Clin Genet. 1974;6(4):289-93 PMID: 4442233
  8. Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
    J Med Genet. 1971 Sep;8(3):358-63 PMID: 5097143
  9. Trisomy 13 with a 13-X translocation.
    Am J Hum Genet. 1974 May;26(3):385-92 PMID: 4133276
  10. Human genetics.
    Annu Rev Genet. 1973;7:435-72 PMID: 4131531
  11. Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes.
    Proc Natl Acad Sci U S A. 1973 Dec;70(12):3395-9 PMID: 4128545
  12. X inactivation in man: a woman with t(Xq--;12q+).
    Am J Hum Genet. 1973 May;25(3):262-70 PMID: 4704858
  13. Cytogenetic and clinical study on 100 cases of primary amenorrhoea.
    Acta Obstet Gynecol Scand Suppl. 1973;:1-78 PMID: 4518464
  14. X-autosome translocation in normal mother and effectively 21-monosomic daughter.
    J Pediatr. 1974 Apr;84(4):539-46 PMID: 4834247
  15. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
    Cytogenet Cell Genet. 1973;12(5):357-66 PMID: 4131091
  16. Evidence for X-X chromosome translocation in humans.
    Ann Hum Genet. 1969 Oct;33(2):117-24 PMID: 5383978
  17. Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.
    J Med Genet. 1970 Mar;7(1):1-4 PMID: 5480961
  18. Non-random late replication of X chromosomes in mules and hinnies.
    Nature. 1971 Jul 30;232(5309):315-9 PMID: 5094835
  19. An inherited X-autosome translocation in man.
    Ann Hum Genet. 1971 Oct;35(2):171-8 PMID: 5159532
  20. Center for Barr body condensation on the proximal part of the human Xq: a hypothesis.
    Chromosoma. 1974 Jan 29;44(4):361-6 PMID: 4134866
  21. Apparently isodicentric but functionally monocentric X chromosome in man.
    Am J Hum Genet. 1974 Jan;26(1):83-92 PMID: 4130093
  22. Banding patterns and autoradiographic studies of cells with an X-autosome translocation.
    Ann Hum Genet. 1973 Jul;37(1):9-12 PMID: 4128188
  23. [Turner syndrome 45,X-46,XXq+].
    Ann Endocrinol (Paris). 1970 Nov-Dec;31(6):1153-5 PMID: 5509948
  24. Gonadal Dysgenesis with Unusual Abnormalities.
    Arch Dis Child. 1965 Jun;40(211):274-9 PMID: 21032420
  25. Fluorescence and Giemsa banding studies of the allocyclic X chromosome in embryonic and adult mouse cells.
    Exp Cell Res. 1973 Mar 30;78(1):127-35 PMID: 4120564
  26. Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.
    Ann Hum Genet. 1967 May;30(4):313-23 PMID: 5619932
  27. X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome.
    Adv Genet. 1970;15:175-259 PMID: 4936423
  28. A marker X chromosome.
    Am J Hum Genet. 1969 May;21(3):231-44 PMID: 5794013
  29. [Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].
    Cytogenetics. 1971;10(2):87-98 PMID: 5098032
  30. Presumptive x-autosome translocation in a cow: preferential inactivation of the normal x chromosome.
    Nature. 1968 Apr 13;218(5137):183-4 PMID: 5645293
  31. Inactivation of the x-chromosome.
    N Engl J Med. 1972 Feb 10;286(6):318-9 PMID: 5061691
  32. The single-active-X: functional differentiation at the chromosome level.
    Natl Cancer Inst Monogr. 1967 Sep;26:327-51 PMID: 4864109
  33. The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis.
    Hereditas. 1970;66(2):287-92 PMID: 5525826
  34. [Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].
    Humangenetik. 1972;14(4):285-99 PMID: 5051752
  35. THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME.
    Lancet. 1963 Aug 24;2(7304):411 PMID: 14044304
  36. Cytogenetics of fifty patients with primary amenorrhea.
    Am J Obstet Gynecol. 1974 May 1;119(1):14-23 PMID: 4820908
  37. Anomalies of development in a girl with unusual sex chromosomal mosaicism.
    J Med Genet. 1967 Dec;4(4):283-7 PMID: 6082908
  38. Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis.
    Cytogenetics. 1967;6(3):254-67 PMID: 6040474
  39. A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
    Cytogenetics. 1964;3:427-40 PMID: 14267135
  40. Genetic activity of sex chromosomes in somatic cells of mammals.
    Philos Trans R Soc Lond B Biol Sci. 1970 Aug 6;259(828):41-52 PMID: 4399067
  41. An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.
    Clin Genet. 1972;3(5):388-95 PMID: 4117330
  42. Possible X-autosomal translocation in a girl with gonadal dysgenesis.
    J Med Genet. 1970 Dec;7(4):402-6 PMID: 5501708
  43. Isochromosome for the short arm of X, a human 46, XXpi syndrome.
    Ann Hum Genet. 1972 Jul;36(1):79-87 PMID: 4656769
  44. [X-CHROMOSOME ANOMALY AND AHAPTOGLOBINEMIA IN HEMOPHILIA A].
    Acta Haematol. 1965 Jan;33:49-56 PMID: 14286001
  45. X-chromosome inactivation and the Xg locus.
    Am J Hum Genet. 1970 Jul;22(4):460-3 PMID: 5432290
  46. [Ring chromosomes and centric fragments in Turner's syndrome].
    Geburtshilfe Frauenheilkd. 1968 Jan;28(1):11-26 PMID: 5668618
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1974-00-00
Pages
1-16
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]