Literature DB >> 7328411

Familial pericentric inversion of chromosome 2.

M S Mattevi, C E Pinheiro, B Erdtmann, R Z Flores, F M Salzano.   

Abstract

A pericentric inversion of chromosome 2 was detected in eight members of a family ascertained via a proband with congenital jejunal atresia born of consanguineous parents. The latter affection was also present in one of his sibs. Microdensitometric analysis of the patterns of G bands of the inverted segment revealed a balanced rearrangement with unusual break points in p12 and q36; the association with the disease is apparently coincidental.

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Year:  1981        PMID: 7328411

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  4 in total

1.  Abnormal chromosome complement resulting from a familial inversion of chromosome 2.

Authors:  S Richter; B Lockwood; D Lockwood; J Allanson
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

2.  Inversion of chromosome 2 (p11p13): frequency and implications for genetic counselling.

Authors:  I M MacDonald; D M Cox
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 3.  Pericentric inversions. Problems and significance for clinical genetics.

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

4.  The significance of pericentric inversions of chromosome 2.

Authors:  M Djalali; P Steinbach; J Bullerdiek; M Holmes-Siedle; M R Verschraegen-Spae; A Smith
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

  4 in total

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