Literature DB >> 4721341

Ribosomal cistrons and acrocentric chromosomes in man.

K Bross, W Krone.   

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Year:  1973        PMID： 4721341     DOI： 10.1007/BF00279033

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  12 in total

1.  THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES.

Authors:  M A FERGUSON-SMITH
Journal:  Cytogenetics       Date:  1964

2.  Dicentric and monocentric Robertsonian translocations in man.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1972

3.  Amplification as a rectification mechanism for the redundant rRNA genes.

Authors:  M Buongiorno-Nardelli; F Amaldi; P A Lava-Sanchez
Journal:  Nat New Biol       Date:  1972-08-02

4.  Location of ribosomal DNA in the human chromosome complement.

Authors:  A S Henderson; D Warburton; K C Atwood
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

5.  Nucleoli and chromosomes: their relationships during the meiotic prophase of the human fetal oocyte.

Authors:  A Stahl; J M Luciani
Journal:  Humangenetik       Date:  1972

6.  On the number of ribosomal RNA genes in man.

Authors:  K Bross; W Krone
Journal:  Humangenetik       Date:  1972

7.  A quantitative assay for DNA-RNA hybrids with DNA immobilized on a membrane.

Authors:  D Gillespie; S Spiegelman
Journal:  J Mol Biol       Date:  1965-07       Impact factor: 5.469

8.  Quantitative studies on the arrangement of human metaphase chromosomes. I. Individual features in the association pattern of the acrocentric chromosomes of normal males and females.

Authors:  K D Zang; E Back
Journal:  Cytogenetics       Date:  1968

9.  The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.

Authors:  T Caspersson; G Lomakka; L Zech
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

10.  Ribonucleic acid-deoxyribonucleic acid hybridization in aqueous solutions and in solutions containing formamide.

Authors:  S Gillespie; D Gillespie
Journal:  Biochem J       Date:  1971-11       Impact factor: 3.857
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  13 in total

1.  Human karyotype polymorphism. III. Routine ank fluorescence microscopic investigation of chromosomes in normal adults and mentally retarded children.

Authors:  A V Mikelsaar; M E Käosaar; S J Tüür; M H Viikmaa; T A Talvik; J Lääts
Journal:  Humangenetik       Date:  1975

2.  Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes.

Authors:  D F Smeets; G F Merkx; A H Hopman
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

3.  Monosomy 21 in a human spontaneous abortus. Morphogenetic disturbances and phenotype at the cellular level.

Authors:  A M Kuliev; K N Grinberg; V I Kukharenko; V P Kulazenko; E A Bogomazov
Journal:  Hum Genet       Date:  1977-09-22       Impact factor: 4.132

4.  Molecular analysis of cloned human 18S ribosomal DNA segments.

Authors:  G N Wilson; B A Hollar; J R Waterson; R D Schmickel
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

5.  Satellite association and variations in length of the nucleolar constriction of normal and variant human G chromosomes.

Authors:  E Orye
Journal:  Humangenetik       Date:  1974

6.  Quantitative studies on the arrangement of human metaphase chromosomes. IV. The association frequency of human acrocentric marker chromosomes.

Authors:  H Zankl; K D Zang
Journal:  Humangenetik       Date:  1974

7.  Genotype and phenotype in human chromosome aberrations and in the minute mutants of Drosophila melanogaster.

Authors:  F Vogel
Journal:  Humangenetik       Date:  1973

8.  Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. I. Comparison of trisomy 21 with balanced translocations t(DqGq).

Authors:  K Bross; H Dittes; W Krone; M Schmid; W Vogel
Journal:  Humangenetik       Date:  1973-12-10

9.  Biochemical and cytogenetic studies on the nucleolus organizing regions (NOR) of man. II. A family with the 15/21 translocation.

Authors:  H Dittes; W Krone; K Bross; M Schmid; W Vogel
Journal:  Humangenetik       Date:  1975

10.  Telomere disruption results in non-random formation of de novo dicentric chromosomes involving acrocentric human chromosomes.

Authors:  Kaitlin M Stimpson; Ihn Young Song; Anna Jauch; Heidi Holtgreve-Grez; Karen E Hayden; Joanna M Bridger; Beth A Sullivan
Journal:  PLoS Genet       Date:  2010-08-12       Impact factor: 5.917
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