Literature DB >> 88409

Cytochemical analysis on a case of familial 17ps.

W Au, J A Witek.   

Abstract

Chromosome 17ps was identified in the mother and daughter but not the father of a normal family with no history of congenital abnormality. In addition to G-band and Ag-NOR staining, previously used to study this abnormality, we applied N-band and C-band techniques. Our results showed that 17ps has no demonstrable ribosomal cistron or constitutive heterochromatin.

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Year:  1979        PMID： 88409     DOI： 10.1007/BF00286904

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  18 in total

1.  Familial occurrence of chromosome variant 17ph+.

Authors:  E Kubień; A Kleczkowska
Journal:  Clin Genet       Date:  1977-07       Impact factor: 4.438

2.  A 17p marker chromosome familial study.

Authors:  M M Sandstrom; E C Jenkins
Journal:  Ann Genet       Date:  1973-12

3.  Chromosome investigation in married couples with repeated spontaneous abortions.

Authors:  M E Käosaar; A V Mikelsaar
Journal:  Humangenetik       Date:  1973

4.  Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Authors:  A V Mikelsaar; S J Tüür; M E Käosaar
Journal:  Humangenetik       Date:  1973

5.  Significance of chromosome 17ps+ in three generations of a family.

Authors:  J H Priest; D C Peakman; S R Patil; A Robinson
Journal:  J Med Genet       Date:  1970-06       Impact factor: 6.318

6.  An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.

Authors:  S E Bloom; C Goodpasture
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

7.  Location of nucleolar organizers in animal and plant chromosomes by means of an improved N-banding technique.

Authors:  K Funaki; S Matsui; M Sasaki
Journal:  Chromosoma       Date:  1975       Impact factor: 4.316

8.  Minor chromosome variations and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls.

Authors:  A T Tharapel; R L Summitt
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132

9.  Assignment of the integration site for simian virus 40 to chromosome 17 in GM54VA, a human cell line transformed by simian virus 40.

Authors:  C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1977-01       Impact factor: 11.205

10.  Silver staining studies on the short arm variant of human chromosome 17.

Authors:  N Oliver; U Francke; K M Taylor
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132
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