Literature DB >> 6228187

Triple chromosome synapsis in oocytes from a human foetus with trisomy 21.

B M Wallace, M A Hultén.   

Abstract

Oocytes from a human foetus with trisomy 21 were spread using detergent and examined by light and electron microscopy. The three chromosomes 21 occurred as bivalent and univalent or trivalent configurations. In the trivalents the lateral elements of the synaptonemal complex were associated in threes, either completely along the length of the trivalent, or partially, forming a variety of forked structures. This triple association demonstrates that, contrary to the classical view of chromosome pairing, three homologous chromosomes can be held in register at the same site.

Entities:  

Mesh:

Year:  1983        PMID: 6228187     DOI: 10.1111/j.1469-1809.1983.tb00996.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  12 in total

1.  Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male.

Authors:  Petrice W Brown; Luann Judis; E Ricky Chan; Stuart Schwartz; Allen Seftel; Anthony Thomas; Terry J Hassold
Journal:  Am J Hum Genet       Date:  2005-08-16       Impact factor: 11.025

2.  Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis.

Authors:  J A Crolla; J F Harvey; F L Sitch; N R Dennis
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

3.  Pachytene chromosomes in trisomy 19 male mice with Robertsonian translocations.

Authors:  R Johannisson; H Winking
Journal:  Chromosome Res       Date:  1998-06       Impact factor: 5.239

4.  The prophase stages in human foetal oocytes studied by light and electron microscopy.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

Review 6.  The genetics of human reproduction.

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

7.  Prophase pairing in a mosaic 18p-;iso 18q human female foetus studied by surface spreading.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

8.  Ovarian dysgenesis in individuals with chromosomal abnormalities.

Authors:  C Cunniff; K L Jones; K Benirschke
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

9.  Meiotic configurations in female trisomy 21 foetuses.

Authors:  R M Speed
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Development of the first meiotic prophase stages in human fetal oocytes observed by light and electron microscopy.

Authors:  M Garcia; A J Dietrich; L Freixa; A C Vink; M Ponsà; J Egozcue
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.