Literature DB >> 5315468

[Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].

G Malpuech, E J Raynaud, J Belin, P Godeneche, J de Grouchy.   

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Year:  1971        PMID： 5315468

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  6 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

4.  Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.

Authors:  C Waldenmaier; W Hirsch; E König; K Shibata
Journal:  Humangenetik       Date:  1974-03-28

Review 5.  The use of new staining techniques for human chromosome identification.

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

6.  18p--syndrome resulting from 14q/18q 'dicentric' fusion translocation.

Authors:  S J Funderburk; R S Sparkes; I Klisak
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132
  6 in total

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