Literature DB >> 4065899

Familial paracentric inversion inv(2)(q31q36).

M Schmid, R Hofmann, J Köhler, U Jannek.   

Abstract

A paracentric inversion of chromosome 2 is described for the first time. The breakpoints were localized in the bands q31 and q36. The paracentric inversion was initially identified in a female with repeated abortions and thereafter detected in eight other family members over three generations. The meiotic consequences and the risk for liveborn unbalanced chromosomal recombinants is discussed.

Mesh：

Year:  1985        PMID： 4065899     DOI： 10.1007/BF00284590

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


  14 in total

1.  The Stability of Broken Ends of Chromosomes in Zea Mays.

Authors:  B McClintock
Journal:  Genetics       Date:  1941-03       Impact factor: 4.562

2.  Familial paracentric inversion of the short arm of chromosome 3.

Authors:  J P Fryns; H van den Berghe
Journal:  Ann Genet       Date:  1979

3.  Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review.

Authors:  E H Mules; J Stamberg
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  A familial paracentric inversion: a short review of the current status.

Authors:  P A Venter; B Dawson; J L Du Toit; E L Smith; N Kritzinger; A S Landman; A S Cronje; J Op't Hof
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Cytogenetic recombinants from a female carrying a paracentric inversion of the short arm of chromosome number 5.

Authors:  E Valcárcel; J Benítez; P Martínez; J A Rey; A Sánchez Cascos
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

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

Authors:  E J Winsor; C G Palmer; P M Ellis; J L Hunter; M A Ferguson-Smith
Journal:  Cytogenet Cell Genet       Date:  1978

7.  Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter).

Authors:  C Trunca; J M Opitz
Journal:  Am J Med Genet       Date:  1977

8.  Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.

Authors:  R S Sparkes; H Muller; I Klisak
Journal:  Science       Date:  1979-03-09       Impact factor: 47.728

9.  Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.

Authors:  H E Wyandt; R Kasprzak; J Ennis; K Willson; V Koch; P Schnatterly; W Wilson; T E Kelly
Journal:  Am J Hum Genet       Date:  1980-09       Impact factor: 11.025

Review 10.  Paracentric inversions in man.

Authors:  K Madan; M Seabright; R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318
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  5 in total

Review 1.  Homozygous paracentric inversion 12 in a mentally retarded boy: a case report and review of the literature.

Authors:  H A Price; S H Roberts; K M Laurence
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

2.  Paracentric inversions in man.

Authors:  J P Fryns; A Kleczkowska; H Van den Berghe
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

Review 3.  Paracentric inversions: a review.

Authors:  K Madan
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

4.  Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities.

Authors:  C C Lin; P Bowen; J J Hoo
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

5.  The Largest Paracentric Inversion, the Highest Rate of Recombinant Spermatozoa. Case Report: 46,XY, inv(2)(q21.2q37.3) and Literature Review.

Authors:  Cc Yapan; C Beyazyurek; Cg Ekmekci; S Kahraman
Journal:  Balkan J Med Genet       Date:  2014-12-11       Impact factor: 0.519
  5 in total

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