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PMID: 4247410 Published · ppublish ger Journal Article

[Tandem chromosome (G-G) with satellites on short and long arm in a patient with trisomy G1].

Tandemchromosom (G-G) mit Satelliten am kurzen und langen Arm bei einem Patienten mit Translokationstrisomie G1.

Humangenetik ·Vol. 9 ·No. 4 ·1970-00-00 ·Pages 361-71

Vogel W, Reinwein H, Engel W

Abstract

暂无摘要

MeSH Terms
Autoradiography Child Chromosome Aberrations Chromosome Mapping Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Cytogenetics Down Syndrome/congenital Humans Karyotyping Male Trisomy
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Vogel W
Reinwein H
Engel W
References (16)
16 references, click to expand
  1. [A case of G-G translocation in tandem].
    Ann Genet. 1965;8(1):60-2 PMID: 5294580
  2. Pericentric inversion in a family with a 21/22 translocation.
    Cytogenetics. 1968;7(2):108-17 PMID: 4231671
  3. PRESUMED TRANSLOCATION OF CHROMOSOME NUMBER 2 AND ONE OF THE D GROUP.
    Cleve Clin Q. 1963 Oct;30:225-32 PMID: 14079210
  4. [Karyotype and phenotype of autosome aberrations in man].
    Veroff Morphol Pathol. 1968;74:1-295 PMID: 4876604
  5. An unusual translocation in a case of Mongolism.
    J Pediatr. 1963 Feb;62:225-9 PMID: 14003439
  6. Chromosome preparations of leukocytes cultured from human peripheral blood.
    Exp Cell Res. 1960 Sep;20:613-6 PMID: 13772379
  7. DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.
    Cytogenetics. 1963;2:175-93 PMID: 14101501
  8. Subglottic pseudotumor, laryngeal dysplasia, and chondrodysplasia calcificans congenita with a t(D;B) chromosomal translocation.
    Ann Genet. 1967 Jun;10(2):55-9 PMID: 5298973
  9. [A female patient with translocation 46, XX, t(Dq-; Bq+) and neurofibromatosis, imbecility and aortic coarctation].
    Schweiz Med Wochenschr. 1969 Feb 8;99(6):182-6 PMID: 4976446
  10. D-E (13-15/17-18) translocation: occurrence in an infant with 45 chromosomes.
    Am J Dis Child. 1965 Dec;110(6):686-8 PMID: 5845212
  11. [Familial D-E translocation].
    Acta Genet Med Gemellol (Roma). 1967 Oct;16(4):365-75 PMID: 5593928
  12. A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism).
    J Pediatr. 1963 Jun;62:890-4 PMID: 13998933
  13. Down's syndrome associated with a familial (21q-; 22q+) translocation.
    Cytogenetics. 1967;6(5):321-30 PMID: 4231490
  14. [Segregation of a D/G translocation "in tandem" in 3 generations].
    Ann Genet. 1966 Sep;9(3):134-6 PMID: 5298292
  15. RECIPROCAL TRANSLOCATION AND MOSAICISM IN A MONGOL.
    J Ment Defic Res. 1965 Jun;9:118-24 PMID: 14323170
  16. The use of perforated cellophane for the growth of cells in tissue culture.
    J Natl Cancer Inst. 1947 Dec;8(3):103-19 PMID: 18902332
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1970-00-00
Pages
361-71
Language
ger
Region
Germany
NLM ID
7607154
Subset
IM
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