Literature DB >> 670937

[Constitutional stereotyped gap in human chromosomes (author's transl)].

B Quack, Y Nantois, J Mottet, B Noël.   

Abstract

The stereotyped break with gap of a chromosomal variant is rarely observed. This anomaly is transmitted according to autosomal dominant rule. The distal part of the broken chromosome may either be still bound to the sister chromatid through mitotic non-disjunction, forming a triradial figure, or take a moniliform and pulverized appearance, evoking premature chromosome condensation.

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Year:  1978        PMID: 670937

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  3 in total

1.  Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites.

Authors:  M Kähkönen; C Tengström; T Alitalo; R Matilainen; M Kaski; E Airaksinen
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

2.  Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency.

Authors:  L Tiepolo; P Maraschio; G Gimelli; C Cuoco; G F Gargani; C Romano
Journal:  Hum Genet       Date:  1979-10-01       Impact factor: 4.132

3.  FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDY.

Authors:  Merlin G Butler
Journal:  J Tenn Acad Sci       Date:  1998 Jul-Oct
  3 in total

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