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86 Possible Causes for Meioses

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  • Classical Phenylketonuria

    No recombination between linked RFLP and the PKU phenotype could be observed in 40 meioses from the investigation of eight families with two affected children each.[]

  • X-Linked Alport Syndrome

    Two large Utah kindreds were included in the genetic studies, kindreds P and C, with 125 and 63 potentially informative meioses, respectively.[]

  • Spondyloepiphyseal Dysplasia Congenita

    No recombinants between the marker and the phenotype were found in eight informative meioses.[]

  • Central Core Disease

    This mutation was linked to CCD with a lod score of 4.8 at a recombinant fraction of 0.0 in 16 informative meioses in a 130 member family, suggesting a causal relationship[]

  • Ocular Albinism

    […] present report, a large South African family with OASD was investigated at the molecular level and tight linkage was found to the DXS452 locus at Xp22.3 using 25 informative meioses[]

  • Åland Islands Eye Disease

    Other positive lod scores at theta max .00 were obtained with markers localized in the XY homologous region in Xq13-q21, but the numbers of informative meioses were small.[]

  • Isolated Ectopia Lentis

    A homozygosity region of 0.67 cM corresponds to approximately 300 meioses (150 generations) back to the most recent common ancestor. 17 The chromosome ideogram and physical[]

  • Heterotaxia

    […] liver; P, pancreas; asterisks denote position of lov expression in the brain. ( g ) The sfw mutation was mapped to linkage group 5. x/96 denotes number of recombinants in 96 meioses[]

  • Catatonic Schizophrenia

    Sharing of common markers of any chromosomal regions divided by only three meioses is expectable for one out of four of all chromosomal loci in such a small family, resulting[]

  • Angioma Serpiginosum

    In the family, 11 informative meioses were available to study the segregation of X-chromosome markers.[] There are 12 informative meioses in the family, of which 11 were available for direct study.[] After determination of haplotypes (phase), there are 11 meioses in which there is an a priori 0.5 chance for separation of the disease and the haplotype under the null-hypothesis[]

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