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PMID: 4647439 Published · ppublish English Journal Article

Spontaneous chromosomal instability.

Humangenetik ·Vol. 16 ·No. 1 ·1972-00-00 ·Pages 151-7

Passarge E

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple Anemia, Aplastic/genetics Ataxia Telangiectasia/genetics Cells, Cultured Chromosomes Dwarfism/genetics Erythema/genetics Facial Dermatoses/genetics Genes, Recessive Humans Karyotyping Lymphocytes Photosensitivity Disorders/genetics Telangiectasis/congenital Time Factors Xeroderma Pigmentosum/genetics
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Passarge E
References (7)
7 references, click to expand
  1. CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN.
    Science. 1965 Apr 23;148(3669):506-7 PMID: 14263770
  2. Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease.
    Blood. 1971 Jan;37(1):96-112 PMID: 5539134
  3. CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.
    Science. 1964 Apr 17;144(3616):298-301 PMID: 14169717
  4. Incidence and mutation rates of structural rearrangements of the autosomes in man.
    Ann Hum Genet. 1972 Mar;35(3):301-19 PMID: 4262869
  5. [Spontaneous chromosome aberrations in familial panmyelopathy].
    Humangenetik. 1964;1(2):194-6 PMID: 5869479
  6. Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.
    Am J Hum Genet. 1969 Mar;21(2):196-227 PMID: 5770175
  7. Genes which increase chromosomal instability in somatic cells and predispose to cancer.
    Prog Med Genet. 1972;8:61-101 PMID: 4557110
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1972-00-00
Pages
151-7
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
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