Literature DB >> 8168812

Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization.

M Guttenbach1, R Schakowski, M Schmid.   

Abstract

Nonradioactive in situ hybridization with an alpha-satellite DNA probe specific for chromosome 18 was performed on human interphase sperm nuclei to detect the frequency of sperm cells disomic for chromosome 18. A total of 16,127 sperm heads from eight healthy donors, aged 23-57 years, was investigated, and a minimum of 2000 sperm nuclei per proband was analyzed. The disomy rate ranged from 0.25% to 0.5%, with an average of 0.36%. This frequency does not differ significantly from that determined for other chromosomes.

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Year:  1994        PMID: 8168812     DOI: 10.1007/bf00201667

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


  18 in total

1.  Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes.

Authors:  R H Martin; E Ko; A Rademaker
Journal:  Am J Med Genet       Date:  1991-06-01

2.  Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei.

Authors:  M Guttenbach; M Schmid
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

3.  Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphism.

Authors:  T Kondoh; H Tonoki; T Matsumoto; M Tsukahara; N Niikawa
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

4.  Parental origin of the extra chromosome in trisomy 18.

Authors:  K G Kupke; U Müller
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

5.  Parental origin of the supernumerary chromosome in trisomy 18.

Authors:  X Ya-gang; W P Robinson; R Spiegel; F Binkert; U Ruefenacht; A A Schinzel
Journal:  Clin Genet       Date:  1993-08       Impact factor: 4.438

6.  Rates of chromosome abnormalities at different maternal ages.

Authors:  E B Hook
Journal:  Obstet Gynecol       Date:  1981-09       Impact factor: 7.661

Review 7.  Trisomy in man.

Authors:  T J Hassold; P A Jacobs
Journal:  Annu Rev Genet       Date:  1984       Impact factor: 16.830

8.  The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements.

Authors:  R H Martin; A Rademaker
Journal:  Cytogenet Cell Genet       Date:  1990

9.  Incidence of chromosome aberrations among 11148 newborn children.

Authors:  J Nielsen; I Sillesen
Journal:  Humangenetik       Date:  1975-10-20

10.  Nonisotopic in situ hybridization as a method for nondisjunction studies in human spermatozoa.

Authors:  E Coonen; M H Pieters; J C Dumoulin; H Meyer; J L Evers; F C Ramaekers; J P Geraedts
Journal:  Mol Reprod Dev       Date:  1991-01       Impact factor: 2.609

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  5 in total

1.  Fluorescence in situ hybridization with chromosome paint probes: a novel approach to assess aneuploidy in human sperm nuclei.

Authors:  N Rives; S Wust; B David; V Duchesne; G Joly; B Mace
Journal:  J Assist Reprod Genet       Date:  1999-01       Impact factor: 3.412

2.  Genetics of human sperm.

Authors:  R H Martin
Journal:  J Assist Reprod Genet       Date:  1998-05       Impact factor: 3.412

3.  Sex chromosomal analysis of spermatozoa from infertile men using fluorescence in situ hybridization.

Authors:  N Nishikawa; I Murakami; K Ikuta; K Suzumori
Journal:  J Assist Reprod Genet       Date:  2000-02       Impact factor: 3.412

4.  Direct detection of disomy in human sperm by the PRINS technique.

Authors:  F Pellestor; I Quennesson; L Coignet; A Girardet; B Andréo; J P Charlieu
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

5.  Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes.

Authors:  S Rousseaux; E Chevret; M Monteil; J Cozzi; R Pelletier; D Delafontaine; B Sèle
Journal:  Hum Genet       Date:  1995-12       Impact factor: 4.132

  5 in total

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