Literature DB >> 648176

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.

E J Winsor, C G Palmer, P M Ellis, J L Hunter, M A Ferguson-Smith.   

Abstract

In a family in which a large pericentric inversion of chromosome 7 is segregating, two of the four progeny of inversion heterozygotes show severe psychomotor retardation and have the karyotype 46,XX,rec(7),dup q,inv(7)(p22q32), derived from crossing-over within the inversion. Meiotic analysis in one of the heterozygotes revealed no evidence of inversion loops in well-spread pachytene cells. In approximately 20% of cells in diakinesis, the presumptive bivalent 7 had only one chiasma. Two alternatives to the reversed loop mode of meiotic pairing of inversions are proposed. Review of the literature supports the view that "small" pericentric inversions have a much better genetic prognosis than "large" pericentric inversions.

Entities:  

Mesh:

Year:  1978        PMID: 648176     DOI: 10.1159/000130849

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  36 in total

1.  A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).

Authors:  A Delicado; E Escribano; I Lopez Pajares; A Diaz de Bustamante; S Carrasco
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

2.  Unusual segregation products in sperm from a pericentric inversion 17 heterozygote.

Authors:  Monica M Mikhaail-Philips; Barbara C McGillivray; Sara J Hamilton; Evelyn Ko; Judy Chernos; Alfred Rademaker; Renée H Martin
Journal:  Hum Genet       Date:  2005-05-28       Impact factor: 4.132

3.  Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

Authors:  G M Brown; M Leversha; M Hulten; M A Ferguson-Smith; N A Affara; R A Furlong
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

4.  De novo inv(17)(p11.2q21.3) in an intellectually disabled girl: appraisal of 21 inv(17) constitutional instances.

Authors:  Miriam Partida-Pérez; María G Domínguez; Vivian Alejandra Neira; Luis E Figuera; Horacio Rivera
Journal:  J Genet       Date:  2012-08       Impact factor: 1.166

Review 5.  Genetic markers on chromosome 7.

Authors:  L C Tsui
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

6.  Chromosome 7 short arm deletion, 7p21----pter.

Authors:  M Schömig-Spingler; M Schmid; W Brosi; T Grimm
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

Review 7.  Pericentric inversions. Problems and significance for clinical genetics.

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

8.  Meiotic exchange and segregation in female mice heterozygous for paracentric inversions.

Authors:  Kara E Koehler; Elise A Millie; Jonathan P Cherry; Stefanie E Schrump; Terry J Hassold
Journal:  Genetics       Date:  2004-03       Impact factor: 4.562

9.  A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21.

Authors:  T Motegi; M Ohuchi; C Ohtaki; K Fujiwara; S Enomoto; T Hasegawa; K Kishi; H Hayakawa
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly.

Authors:  M J Faed; M A Lamont; K Baxby
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.