Literature DB >> 7449177

Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11 leads to q13) segment of chromosome 2.

C Baccichetti, E Lenzini, A Peserico, R Tenconi.   

Abstract

Pericentric inversion of chromosome 2 was detected in four unrelated families. All these inversions involved the segment p11 leads to q13. The pedigree data are considered in comparison with other cases reported in the literature. Segregation data and possible reproductive failures are discussed.

Entities:  

Mesh：

Year:  1980        PMID： 7449177     DOI： 10.1111/j.1399-0004.1980.tb01783.x

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


  7 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

3.  Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems.

Authors:  D R Romain; C J Chapman; L Columbano-Green; R H Smythe; O Gebbie
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

4.  Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families.

Authors:  C Baccichetti; R Tenconi; D Caufin; L Bortotto
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 5.  Pericentric inversions. Problems and significance for clinical genetics.

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

6.  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

Review 7.  Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.

Authors:  R Pallotta
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318
  7 in total

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