Literature DB >> 130624

[Cytogenetic studies in four cases of Fanconi's anemia (author's transl)].

R Berger, A Bussel, C Schenmetzler.   

Abstract

In two sibships, four patients with Fanconi's anaemia were studied cytogenetically. Interfamilial variations of the frequency of chromosome breakage and rearrangements were found, suggesting the heterogeneity of the disease. Variations of chromosomal abnormalities have also been found during the course of the disease. An abnormal 47 chromosomes clone has been observed in the bone marrow cells from one patient. A mechanism of somatic segregation is probably involved in the constitution of that clone.

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Year:  1975        PMID: 130624

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol        ISSN: 0029-4810


  3 in total

1.  Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia.

Authors:  J L Huret; E Benz; F Guilhot; A Brizard; J Tanzer
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

2.  Spectrum of anomalies in Fanconi anaemia.

Authors:  A Glanz; F C Fraser
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

3.  Chromosomal studies of leukemic and preleukemic Fanconii's anemia patients: examples of acquired 'chromosomal amplification.'.

Authors:  R Berger; A Bernheim; M Le Coniat; D Vecchione; G Schaison
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  3 in total

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