Literature DB >> 7203485

Nonrandom distribution of exchange points in patients with reciprocal translocations.

C Stoll.   

Abstract

A total of 770 breakpoints (80 of them identified by the authors) from unrelated patients with two-break rearrangements resulting in reciprocal translocations were studied to determine whether they were located preferentially. The distribution of breakpoints among the chromosome arms differs from that expected on the basis of their lengths, with more than expected on chromosome arms 4p, 9p, 9q, 13q, 18q, 21p, 21q, 22p, and 22q and fewer than expected on 1p, 1q, 3p, 3q, 5q, 6q, 7p, 12p, 16p, and the gonosomes. More breakpoints than expected occurred in the centromeric regions, and fewer in the median regions. Distribution of breakpoints within bands differed with the technique used: with G banding a many more breakpoints were localized in the light bands and fewer in the dark bands. With R banding no fewer than expected were present in the light bands and only slightly more were found in the dark bands.

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Year:  1980        PMID: 7203485     DOI: 10.1007/bf00281575

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


  25 in total

1.  Balanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl.

Authors:  C Stoll; J M Levy; M Champy
Journal:  Humangenetik       Date:  1975

2.  Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors:  Y Nakagome; H Chiyo
Journal:  Am J Hum Genet       Date:  1976-01       Impact factor: 11.025

3.  Localization of gamma-rays induced chromatid breaks using a three consecutive staining technique.

Authors:  C Dubos; E V Pequignot; B Dutrillaux
Journal:  Mutat Res       Date:  1978-01       Impact factor: 2.433

4.  [De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].

Authors:  C Stoll; J M Levy
Journal:  Ann Genet       Date:  1974-09

5.  Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocations.

Authors:  C Stoll; E Flori; J Macler; R Renaud
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

6.  Localization of sister chromatid exchanges in human chromosomes.

Authors:  S A Latt
Journal:  Science       Date:  1974-07-05       Impact factor: 47.728

7.  High resolution studies on the pattern of induced exchanges in the human karyotype.

Authors:  M Seabright
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

8.  Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes.

Authors:  M Holmberg; J Jonasson
Journal:  Hereditas       Date:  1973       Impact factor: 3.271

9.  Radiation-induced non-random chromosome breakage.

Authors:  T Caspersson; U Haglund; B Lindell; L Zech
Journal:  Exp Cell Res       Date:  1972-12       Impact factor: 3.905

10.  [Chromatid exchanges in human mitotic cells. BUDR Treatment and bichromatic fluorescence by aridine orange (author's transl)].

Authors:  B Dutrillauz; A M Fosse; M Prieur; J Lejeune
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

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  10 in total

1.  The association of t (13q, 14q) with Down's syndrome and its inheritance.

Authors:  T Sudha; S Jayam; R Ramachandran
Journal:  Indian J Pediatr       Date:  1990 Mar-Apr       Impact factor: 1.967

2.  Partial trisomy 12q24.31----qter.

Authors:  E H Tajara; M Varella-Garcia; A C Gusson
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

3.  Cytogenetic survey in couples with recurrent fetal wastage.

Authors:  J P Fryns; A Kleczkowska; E Kubień; P Petit; H Van den Berghe
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes.

Authors:  R S Young; T Reed; M E Hodes; C G Palmer
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  Hotspots of mutation and breakage in dog and human chromosomes.

Authors:  Caleb Webber; Chris P Ponting
Journal:  Genome Res       Date:  2005-12       Impact factor: 9.043

Review 6.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 7.  Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.

Authors:  A O Wilkie
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

8.  Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

Authors:  J P Fryns; A Kleczkowska; E Kubień; H Van den Berghe
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

9.  The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Authors:  R H Lindenbaum; M Hultén; A McDermott; M Seabright
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

Review 10.  Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature.

Authors:  Brian P Brooks; Jeanne M Meck; Bassem R Haddad; Claude Bendavid; Delphine Blain; Jeffrey A Toretsky
Journal:  BMC Med Genet       Date:  2006-01-13       Impact factor: 2.103

  10 in total

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