Literature DB >> 6714976

Familial inv(1) (p3500q21.3) associated with azoospermia.

H Rivera, M C Alvarez-Arratia, M Moller, M Díaz, J M Cantú.   

Abstract

An inv(1) (p3500q21.3) was found in an azoospermic man, his mother and two other maternal relatives. Although the mechanisms involved are still unclear, it is stressed that pericentric inversions of chromosome 1 in which the inverted chromosome becomes submetacentric (centromeric index less than or equal to 0.324) apparently impair spermatogenesis.

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Year:  1984        PMID: 6714976     DOI: 10.1007/bf00286593

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  38 in total

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Authors:  F Giraud; J F Mattei; M G Mattei; S Ayme
Journal:  J Genet Hum       Date:  1979-06

2.  200 infertile males: correlation of chromosome, histological, endocrine and clinical studies.

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4.  Meiotic studies of translocations causing male sterility in the mouse. I. Autosomal reciprocal translocations.

Authors:  J Forejt; S Gregorová
Journal:  Cytogenet Cell Genet       Date:  1977

5.  Familial pericentric inversion of chromosome 1 with a note on reproductive risks.

Authors:  P N Howard-Peebles
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

6.  Structural differences in pericentric inversions. Application to a model of risk of recombinants.

Authors:  A Daniel
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Familial pericentric inversion of chromosome 1 in a boy with Goldenhar's syndrome.

Authors:  C Stahl-Maugé; P Weiss-Wichert; P Propping
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

Authors:  A Joseph; I M Thomas
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

Review 9.  The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

Authors:  E Lifschytz; D L Lindsley
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

10.  Meiosis in two human reciprocal translocations.

Authors:  C S Román; M T Sordo; J M García-Sagredo
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

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  6 in total

1.  Familial inv(1)(p36.3q12) associated with sterility.

Authors:  A Barros; M C Tavares; M P Gomes; M P Tavares
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

2.  Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest.

Authors:  D Meschede; U G Froster; M Bergmann; E Nieschlag
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

3.  Pericentric inversion in human chromosome 1 and the risk for male sterility.

Authors:  A C Chandley; S McBeath; R M Speed; L Yorston; T B Hargreave
Journal:  J Med Genet       Date:  1987-06       Impact factor: 6.318

4.  Familial pericentric and paracentric inversions of chromosome 1.

Authors:  D D Johnson; W B Dobyns; H Gordon; G W Dewald
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

5.  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

6.  Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect.

Authors:  J Batanian; M A Hulten
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

  6 in total

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