Literature DB >> 5459851

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

T Caspersson, J Lindsten, L Zech.   

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Year:  1970        PMID： 5459851     DOI： 10.1016/0014-4827(70)90479-9

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN： 0014-4827            Impact factor:   3.905


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  7 in total

1.  A strongly fluorescing abnormal chromosome in a malformed child.

Authors:  E M Bühler; H Müller; G R Stalder; E Werder
Journal:  Humangenetik       Date:  1971

2.  [Fluorescent microscopy detection of human Y-chromosome in interphase nuclei using acridine derivatives ("atebrin", "acranil")].

Authors:  F Majewski; L Bier; R A Pfeiffer
Journal:  Klin Wochenschr       Date:  1971-07-15

3.  Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

Authors:  U Francke
Journal:  Am J Hum Genet       Date:  1972-03       Impact factor: 11.025

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

Authors:  M Bobrow; P L Pearson
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

Review 5.  Chromosome studies in man: past achievements and recent advances.

Authors:  S D Lawler; B R Reeves
Journal:  J Clin Pathol       Date:  1976-07       Impact factor: 3.411

6.  Cytologic observations in 35 individuals with a 5p- karyotype.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

Review 7.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132
  7 in total

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