Literature DB >> 6074579

Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia.

W Schmid.   

Abstract

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Year:  1967        PMID： 6074579

Source DB:  PubMed          Journal:  Semin Hematol        ISSN： 0037-1963            Impact factor:   3.851


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  6 in total

1.  Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.

Authors:  M J Shahid; F P Khouri; S K Ballas
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

2.  Cytogenetical and clinical investigations in aplastic anaemia (Fancomi's type).

Authors:  G Guanti; P Petrinelli; F Schettini
Journal:  Humangenetik       Date:  1971

3.  Localization chromatid breaks in Fanconi's anemia, using three consecutive stains.

Authors:  B Dutrillaux; J Couturier; E Viegas-Péquignot; G Schaison
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

4.  Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts.

Authors:  M C Yoshida
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.

Authors:  O Mutchinick; L Ruz; M E Gonsebatt; P Mauleón; R Lisker; G García
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  A case of pure red cell aplasia with a high incidence of spontaneous chromosome breakage: a possible X-ray sensitive syndrome.

Authors:  O Iskandar; M J Jager; R Willenze; A T Natarajan
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132
  6 in total

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