Literature DB >> 1175321

The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results.

P A Jacobs, A Frackiewicz, P Law, C J Hilditch, N E Morton.   

Abstract

Reproductive fitness was measured in the following seven classes of pedigrees: (1) D/D Robertsonian translocations ascertained through a euploid proband; (2) D/G Robertsonian translocations ascertained through a euploid proband: (3) reciprocal translocations ascertained through a euploid proband; (4) inversions ascertained through a euploid proband; (5) all translocations and inversions ascertained through an aneuploid proband; (6) those ascertained through a proband with a ring, marker, or supernumerary chromosome; (7) those ascertained through a proband with an extreme variant chromosome. For each group reproductive fitness was calculated in two ways. One method was based on live births, fetal and infant deaths and generation time of those individuals carrying a chromosome abnormality or variant by comparison with their first degree relatives who were known to have a normal chromosome constitution. The second method was based on the proportion of sporadic cases obtained from segregation analysis. The results obtained using both methods are presented and discussed.

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Year:  1975        PMID: 1175321     DOI: 10.1111/j.1399-0004.1975.tb01490.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  33 in total

1.  Investigation of the origins of human autosomal inversions.

Authors:  N Simon Thomas; Victoria Bryant; Vivienne Maloney; Annette E Cockwell; Patricia A Jacobs
Journal:  Hum Genet       Date:  2008-05-10       Impact factor: 4.132

2.  Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome.

Authors:  S A Goodart; M G Butler; J Overhauser
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

3.  A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences.

Authors:  L Doneda; P Gandolfi; G Nocera; L Larizza
Journal:  Chromosome Res       Date:  1998-08       Impact factor: 5.239

4.  A closer look at chromosomal inversions.

Authors:  P S Moorhead
Journal:  Am J Hum Genet       Date:  1976-05       Impact factor: 11.025

5.  Characterization of a (Y;4) translocation by DNA hybridization.

Authors:  M Andersson; D C Page; L G Brown; K Elfving; A de la Chapelle
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

6.  Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping.

Authors:  B Trask; G van den Engh; B Mayall; J W Gray
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

7.  Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans.

Authors:  Mette Gilling; Jörn S Dullinger; Stefan Gesk; Simone Metzke-Heidemann; Reiner Siebert; Thomas Meyer; Karen Brondum-Nielsen; Niels Tommerup; Hans-Hilger Ropers; Zeynep Tümer; Vera M Kalscheuer; N Simon Thomas
Journal:  Am J Hum Genet       Date:  2006-03-17       Impact factor: 11.025

8.  Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6.

Authors:  E W Jabs; N Carpenter
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

Review 9.  Pericentric inversions. Problems and significance for clinical genetics.

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

10.  C heterochromatin variation in couples with recurrent early abortions.

Authors:  A Maes; C Staessen; L Hens; E Vamos; M Kirsch-Volders; M C Lauwers; E Defrise-Gussenhoven; C Susanne
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

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