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  • Articles: DFG German National Licenses  (2)
  • 1985-1989  (2)
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  • Articles: DFG German National Licenses  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 442 (1985), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Notes: It appears that the chance of an in vitro fertilization (IVF) embryo to produce a pregnancy carried to term is about 10%.1 Consequently, one of the most important factors in increasing the pregnancy rate after in vitro fertilization and embryo transfer is replacement of multiple embryos.2 When we consider that the estimated human fecundity rate is about 25%,3 it seems likely that the quality of the embryo is one determining factor for a successful pregnancy rate. Different types of defects of gametes and embryos might contribute to the explanation of why the vast majority of IVF embryos do not give rise to any sign of pregnancy after replacement.It is well documented that chromosomal abnormalities among first trimester spontaneous abortions occur at a rate of about 60%, indicating that chromosomal abnormalities might be common in human gametes and early development stages.4 Abnormal karyotypes found were aneuploidy (i.e., complements with one extra or one missing chromosome) and polyploidy.Recently, a new technique allowing direct analysis of the chromosomal constitution of human spermatozoa has been reported.5 This technique utilizes the ability of capacitated human spermatozoa to penetrate zona-free hamster oocytes. Five to 10% of penetrating human spermatozoa have shown chromosomal abnormalities. Various degrees of hyperploidy and hypoploidy ranging from three extra to three missing chromosomes were found in a series of 1000 human spermatozoal chromosome constitutions.6 It is interesting to note that among spontaneous first trimester abortions such serious numerical abnormalities have not been found.4
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Genetica 74 (1987), S. 143-147 
    ISSN: 1573-6857
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The karyotype of the osprey consists of 74 chromosomes. There are no large macrochromosomes and no typical microchromosomes. Autosome No. 2 has a prominent secondary constriction in the long arm. The Z chromosome is similar in size and shape to the largest autosome, the W is a small metacentric. Among the Falconiformes, the osprey karyotype mainly resembles the karyotypes of some accipitrid species. However, certain characteristic features of the karyotype, a unique secondary constriction chromosome and absence of microchromosomes, speak in favour of maintaining the osprey in a family of its own, Pandionidae.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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