Literature DB >> 5703223

Human ring chromosome syndromes. An "E" ring associated with an abnormal phenotype.

A K Sinha.   

Abstract

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Year:  1968        PMID: 5703223     DOI: 10.1017/s1120962300012658

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN: 0001-5660


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  5 in total

Review 1.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 2.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

3.  Ring chromosome 18 (46, XX, 18r).

Authors:  A Cenani; R A Pfeiffer; H A Simon
Journal:  Humangenetik       Date:  1969

4.  Comparative behavior of ring chromosomes.

Authors:  M L Kistenmacher; H H Punnett
Journal:  Am J Hum Genet       Date:  1970-05       Impact factor: 11.025

5.  Median facial cleft associated with ring E chromosome.

Authors:  K W Dumars; L G Carnahan; R V Barrett
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

  5 in total

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