Literature DB >> 5096549

The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities.

M Bobrow, P L Pearson.   

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Year:  1971        PMID: 5096549      PMCID: PMC1469005          DOI: 10.1136/jmg.8.2.240

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  4 in total

1.  Identification of human chromosomes by DNA-binding fluorescent agents.

Authors:  T Caspersson; L Zech; C Johansson; E J Modest
Journal:  Chromosoma       Date:  1970       Impact factor: 4.316

2.  Technique for identifying Y chromosomes in human interphase nuclei.

Authors:  P L Pearson; M Bobrow; C G Vosa
Journal:  Nature       Date:  1970-04-04       Impact factor: 49.962

3.  Quinacrine mustard-fluorescence of human chromosomes 4, 5 and X.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-08       Impact factor: 3.905

4.  Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence.

Authors:  T Caspersson; J Lindsten; L Zech
Journal:  Exp Cell Res       Date:  1970-08       Impact factor: 3.905

  4 in total
  6 in total

Review 1.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

2.  A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype.

Authors:  A Carnevale; L De los Cobos
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

3.  Immunoglobulin abnormality in a girl with a large chromosome 18.

Authors:  S Yanagisawa
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

Review 4.  The use of new staining techniques for human chromosome identification.

Authors:  P Pearson
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

5.  Identification of group'E' chromosome abnormalities in human cells.

Authors:  K E Vause; J K McDougall
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

6.  A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.

Authors:  R H Lindenbaum; N L Blackwell; D J De Sa'
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

  6 in total

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