Literature DB >> 7013647

The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human population.

A C Chandley.   

Abstract

It is estimated that perhaps 20 per cent or more of all human conceptuses carry of chromosomal abnormality. This level of abnormality would appear to be higher by an order of magnitude, than that recorded for any other investigated mammalian species. Elimination by spontaneous abortion, miscarriage and peri-natal death accounts for the vast majority of chromosomally-abnormal human conceptuses. Even those individuals who survive into adulthood carrying a chromosome abnormality do so with only a limited potential to pass on their abnormality to their offspring. Some are sterilized by the chromosome abnormalities which they carry, others are mentally incapacitated and therefore excluded from the pool of reproductively active individuals. Among those who can reproduce, chromosomally normal children are usually produced since meiotic drive mechanisms which ensure a chromosomally balanced complement in egg or sperm appear to be operative.

Entities:  

Mesh:

Year:  1981        PMID: 7013647

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  19 in total

1.  Parental age and the origin of trisomy 21. A study of 302 families.

Authors:  F Dagna Bricarelli; M Pierluigi; M Landucci; A Arslanian; D A Coviello; M A Ferro; P Strigini
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

2.  Autosomal trisomy in a heifer.

Authors:  A Mäkinen; I Alitalo; M Alanko
Journal:  Acta Vet Scand       Date:  1987       Impact factor: 1.695

Review 3.  The genetics of human reproduction.

Authors:  A C Chandley
Journal:  Experientia       Date:  1986-10-15

Review 4.  Some trends in medical populations genetics.

Authors:  J Feingold; J L Serre; P Carnevale
Journal:  Experientia       Date:  1986-10-15

5.  Familial inv(1) (p3500q21.3) associated with azoospermia.

Authors:  H Rivera; M C Alvarez-Arratia; M Moller; M Díaz; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Meiotic studies in a series of 1100 infertile and sterile males.

Authors:  J Egozcue; C Templado; F Vidal; J Navarro; F Morer-Fargas; S Marina
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype.

Authors:  D A Laurie; R W Palmer; M A Hultén
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  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

9.  Ring chromosome 21 in healthy persons: different consequences in females and in males.

Authors:  B Dallapiccola; V De Filippis; A Notarangelo; G Perla; L Zelante
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

10.  Prophase of meiosis in human spermatocytes analysed by EM microspreading in infertile men and their controls and comparisons with human oocytes.

Authors:  R M Speed; A C Chandley
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

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