Literature DB >> 7418257

Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6.

R J Schroer, D M Culp, R E Stevenson, W E Potts, H A Taylor, R J Simensen.   

Abstract

A case of trisomy for a portion of the long arm of chromosome 6, secondary to recombination of a maternal pericentric inversion, is presented. The pericentric inversion was documented in three generations of a family with a number of spontaneous abortions and periinatal deaths.

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Year:  1980        PMID： 7418257     DOI： 10.1111/j.1399-0004.1980.tb01369.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  3 in total

1.  The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation.

Authors:  A Schmidt
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 2.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  Pericentric inversions in man: personal experience and review of the literature.

Authors:  A Kleczkowska; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132
  3 in total

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