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PMID: 5051752 Published · ppublish ger Journal Article

[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].

Gonadendysgenesie mit ungewöhnlicher Strukturanomalie eines X-Chromosomes (45,X-46,XXq+.

Humangenetik ·Vol. 14 ·No. 4 ·1972-00-00 ·Pages 285-99

Dollmann A, Nocke W, Stengel-Rutkowski S

Abstract

暂无摘要

MeSH Terms
Adult Amenorrhea/etiology Autoradiography Chromosome Aberrations Female Humans Karyotyping Models, Biological Mosaicism Mouth Mucosa/anatomy & histology Ovary/abnormalities Sex Chromatin/analysis Turner Syndrome/complications,genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dollmann A
Nocke W
Stengel-Rutkowski S
References (29)
29 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. The occurrence of sex chromatin in early human and macaque embryos.
    J Anat. 1957 Jul;91(3):369-73 PMID: 13448995
  3. Evidence for X-X chromosome translocation in humans.
    Ann Hum Genet. 1969 Oct;33(2):117-24 PMID: 5383978
  4. [Tandem chromosome (G-G) with satellites on short and long arm in a patient with trisomy G1].
    Humangenetik. 1970;9(4):361-71 PMID: 4247410
  5. Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome.
    Nature. 1966 Oct 8;212(5058):153-5 PMID: 5972207
  6. [Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].
    Cytogenetics. 1971;10(2):87-98 PMID: 5098032
  7. [Heterosome fragments in gonadal dysgenesis. A contribution on the karyotype--phenotype relationship].
    Klin Wochenschr. 1967 Dec 15;45(24):1225-33 PMID: 5592459
  8. HUMAN SEX CHROMOSOME ABNORMALITIES IN RELATION TO DNA REPLICATION AND HETEROCHROMATINIZATION.
    Proc Natl Acad Sci U S A. 1963 May;49(5):581-9 PMID: 16591069
  9. Chromosome preparations of leukocytes cultured from human peripheral blood.
    Exp Cell Res. 1960 Sep;20:613-6 PMID: 13772379
  10. THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME.
    Lancet. 1963 Aug 24;2(7304):411 PMID: 14044304
  11. BIOMETRICS OF THE KARYOTYPE OF PROTEMNODON BICOLOR, WITH REFERENCE TO THE LIMITATIONS IN ACCURACY OF IDENTIFYING HUMAN CHROMOSOMES.
    Nature. 1963 Oct 19;200:234-7 PMID: 14081059
  12. [RING CHROMOSOMES IN GONADAL DYSGENESIS].
    Geburtshilfe Frauenheilkd. 1964 Mar;24:173-84 PMID: 14164433
  13. A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
    Cytogenetics. 1964;3:427-40 PMID: 14267135
  14. [Ring chromosomes and centric fragments in Turner's syndrome].
    Geburtshilfe Frauenheilkd. 1968 Jan;28(1):11-26 PMID: 5668618
  15. Mammalian X-chromosome action: inactivation limited in spread and region of origin.
    Science. 1963 May 31;140(3570):976-8 PMID: 13975649
  16. [Cytogenetic variation of the Ullrich-Turner syndrome].
    Med Klin. 1968 May 24;63(21):836-41 PMID: 5697511
  17. 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
  18. [THE EXCRETION OF PITUITARY GONADOTROPINS IN WOMEN WITH DISORDERS OF THE OVARIAN FUNCTION BEFORE AND AFTER TREATMENT WITH CLOMIPHENE (MRL-41)].
    Klin Wochenschr. 1964 Jan 1;42:15-21 PMID: 14124049
  19. 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
  20. Sex chromatin and gene action in the mammalian X-chromosome.
    Am J Hum Genet. 1962 Jun;14:135-48 PMID: 14467629
  21. On isopycnotic behavior of the XX-bivalent in oocytes of Rattus norvegicus.
    Exp Cell Res. 1960 Apr;19:637-9 PMID: 14428475
  22. [Turner syndrome 45,X-46,XXq+].
    Ann Endocrinol (Paris). 1970 Nov-Dec;31(6):1153-5 PMID: 5509948
  23. Gonadal Dysgenesis with Unusual Abnormalities.
    Arch Dis Child. 1965 Jun;40(211):274-9 PMID: 21032420
  24. DNA CONTENT AND AREA OF SEX CHROMATIN IN SUBJECTS WITH STRUCTURAL AND NUMERICAL ABERRATIONS OF THE X CHROMOSOME.
    Cytogenetics. 1965;4:96-116 PMID: 14319242
  25. Cytogenetics of abnormal sexual development in man.
    Br Med Bull. 1961 Sep;17:206-12 PMID: 13711654
  26. Anomalies of development in a girl with unusual sex chromosomal mosaicism.
    J Med Genet. 1967 Dec;4(4):283-7 PMID: 6082908
  27. Abnormalities involving the X chromosome in women.
    Lancet. 1960 Jun 4;1(7136):1213-6 PMID: 14406379
  28. Possible X-autosomal translocation in a girl with gonadal dysgenesis.
    J Med Genet. 1970 Dec;7(4):402-6 PMID: 5501708
  29. [X-CHROMOSOME ANOMALY AND AHAPTOGLOBINEMIA IN HEMOPHILIA A].
    Acta Haematol. 1965 Jan;33:49-56 PMID: 14286001
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
DOI
10.1007/BF00290170
Published
1972-00-00
Pages
285-99
Language
ger
Region
Germany
NLM ID
7607154
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00290170
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