Literature DB >> 77246

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

N Oliver, U Francke, K M Taylor.   

Abstract

The absence of silver grain precipitation on human chromosome 17, consistently observed in four patients displaying the 17p variant, supports the hypothesis that the 17p variant is a structural heteromorphism rather than translocated satellite material.

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Year:  1978        PMID: 77246     DOI: 10.1007/BF00291628

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


  9 in total

1.  A 17p marker chromosome familial study.

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

2.  A homozygous chromosomal variant.

Authors:  J M Berg; J A Faunch; M J Pendrey; L S Penrose; M A Ridler; A Shapiro
Journal:  Lancet       Date:  1969-03-08       Impact factor: 79.321

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.  Structural polymorphism in chromosome 17.

Authors:  E Schmid; M Bauchinger
Journal:  Nature       Date:  1969-01-25       Impact factor: 49.962

7.  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

8.  Visualization of nucleolar organizer regions im mammalian chromosomes using silver staining.

Authors:  C Goodpasture; S E Bloom
Journal:  Chromosoma       Date:  1975-11-20       Impact factor: 4.316

9.  Human nucleolar organizer chromosomes: satellite associations.

Authors:  T E Denton; W M Howell; J V Barrett
Journal:  Chromosoma       Date:  1976-03-31       Impact factor: 4.316

  9 in total
  3 in total

1.  The fragile site (17)(p12): induction by AT-specific DNA-ligands and population cytogenetics.

Authors:  M Schmid; W Feichtinger; C Deubelbeiss; E Weller
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

2.  Heritable fragile sites on human chromosomes. IV. Silver staining.

Authors:  G R Sutherland; P Leonard
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

3.  Cytochemical analysis on a case of familial 17ps.

Authors:  W Au; J A Witek
Journal:  Hum Genet       Date:  1979-04-27       Impact factor: 4.132

  3 in total

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