Literature DB >> 3746835

A paracentric inversion of 7q illustrating a possible interchromosomal effect.

J L Watt, K Ward, D A Couzin, G S Stephen, A Hill.   

Abstract

A family is described in which the proband has a rearranged X chromosome involving monosomy Xp and trisomy Xq, while the mother has a paracentric inversion of chromosome 7. It is suggested that the phenomenon of interchromosomal effect may link these observations. A brief review of the published and computer catalogued data on paracentric inversion in man is included.

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Year:  1986        PMID： 3746835      PMCID： PMC1049702          DOI： 10.1136/jmg.23.4.341

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  13 in total

Review 1.  AUTOSOMAL DISORDERS.

Authors:  J LEJEUNE
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

2.  Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.

Authors:  C del Solar; I A Uchida
Journal:  J Pediatr       Date:  1974-04       Impact factor: 4.406

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.  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

5.  Peri- and paracentric inversions in chromosome 12: prenatal diagnosis and family study.

Authors:  H Poulsen; M Mikkelsen; G Holmgren
Journal:  Prenat Diagn       Date:  1981-01       Impact factor: 3.050

6.  Paracentric Inversion in man: personal experience and review of the literature.

Authors:  J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY,inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3).

Authors:  N Canki; B Dutrillaux
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

8.  Systematic analysis of 95 reciprocal translocations of autosomes.

Authors:  A Aurias; M Prieur; B Dutrillaux; J Lejeune
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

9.  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

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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  4 in total

1.  Paracentric inversion of chromosome 15(q15q24): description of three families.

Authors:  E D'Alessandro; C De Matteis; M L Lo Re; M Di Cola; C Ligas; F Cappa; G Del Porto
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

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

Review 3.  Genetic markers on chromosome 7.

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

Review 4.  Paracentric inversions: a review.

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

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