Pages that link to "Q34403129"
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The following pages link to Recombination and nondisjunction in humans and flies (Q34403129):
Displaying 50 items.
- A new genetic linkage map of the zygomycete fungus Phycomyces blakesleeanus (Q21133625) (← links)
- EVOLUTION OF SEXRESOLVING THE PARADOX OF SEX AND RECOMBINATION (Q22121995) (← links)
- The kinetochore prevents centromere-proximal crossover recombination during meiosis (Q27935580) (← links)
- BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism (Q28264465) (← links)
- Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice (Q28506066) (← links)
- To err (meiotically) is human: the genesis of human aneuploidy (Q29618613) (← links)
- Multipoint estimation of genetic maps for human trisomies with one parent or other partial data (Q30587139) (← links)
- Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. (Q30827295) (← links)
- Topological Data Analysis Generates High-Resolution, Genome-wide Maps of Human Recombination (Q31110726) (← links)
- Frequency of aneuploidy in sperm from patients with extremely severe male factor infertility (Q31161829) (← links)
- Mapping meiotic single-strand DNA reveals a new landscape of DNA double-strand breaks in Saccharomyces cerevisiae (Q33310052) (← links)
- New insights into human nondisjunction of chromosome 21 in oocytes (Q33325904) (← links)
- Temporal characterization of homology-independent centromere coupling in meiotic prophase (Q33567702) (← links)
- Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data (Q33643852) (← links)
- Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? (Q33681527) (← links)
- Changing partners: moving from non-homologous to homologous centromere pairing in meiosis (Q33817094) (← links)
- Examining variation in recombination levels in the human female: a test of the production-line hypothesis (Q33858796) (← links)
- Use of a recombination reporter insert to define meiotic recombination domains on chromosome III of Saccharomyces cerevisiae (Q33958581) (← links)
- Fission yeast homologs of human CENP-B have redundant functions affecting cell growth and chromosome segregation (Q33962852) (← links)
- The Evolution of Recombination: Removing the Limits to Natural Selection (Q33971025) (← links)
- Genomic Structure of and Genome-Wide Recombination in the Saccharomyces cerevisiae S288C Progenitor Isolate EM93 (Q34038068) (← links)
- Trisomic pregnancy and earlier age at menopause (Q34142108) (← links)
- High resolution analysis of meiotic chromosome structure and behaviour in barley (Hordeum vulgare L.). (Q34326234) (← links)
- Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes (Q34390520) (← links)
- Short- and long-term effects of chromosome mis-segregation and aneuploidy (Q34486530) (← links)
- A candidate recombination modifier gene for Zea mays L (Q34606249) (← links)
- Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster (Q34607545) (← links)
- Centromere mapping functions for aneuploid meiotic products: Analysis of rec8, rec10 and rec11 mutants of the fission yeast Schizosaccharomyces pombe (Q34607587) (← links)
- Meiotic chromosome dynamics dependent upon the rec8(+), rec10(+) and rec11(+) genes of the fission yeast Schizosaccharomyces pombe (Q34607612) (← links)
- The evolution of recombination in a heterogeneous environment. (Q34610474) (← links)
- Chromosomal rearrangements and evolution of recombination: comparison of chiasma distribution patterns in standard and robertsonian populations of the house mouse (Q34616414) (← links)
- American College of Medical Genetics statement of diagnostic testing for uniparental disomy (Q35034233) (← links)
- High throughput sequencing reveals alterations in the recombination signatures with diminishing Spo11 activity (Q35034403) (← links)
- Chromosomal drive and the evolution of meiotic nondisjunction and trisomy in humans (Q35916406) (← links)
- The control of mammalian female meiosis: factors that influence chromosome segregation (Q36267589) (← links)
- The effects of anticancer drugs TSA and GSK on spermatogenesis in male mice (Q36595148) (← links)
- Genetic Background, Maternal Age, and Interaction Effects Mediate Rates of Crossing Over in Drosophila melanogaster Females (Q36867950) (← links)
- Conserved Genetic Architecture Underlying Individual Recombination Rate Variation in a Wild Population of Soay Sheep (Ovis aries) (Q36875722) (← links)
- Absence of age effect on meiotic recombination between human X and Y chromosomes (Q37217927) (← links)
- Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction (Q37219944) (← links)
- Emerging roles for centromeres in meiosis I chromosome segregation (Q37256638) (← links)
- Variation and Evolution of the Meiotic Requirement for Crossing Over in Mammals (Q37576467) (← links)
- Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. (Q37587521) (← links)
- Molecular insights into the aetiology of female reproductive ageing. (Q38605681) (← links)
- Chromosome abnormalities in human beings. (Q40872596) (← links)
- Centromeres, checkpoints and chromatid cohesion. (Q41441718) (← links)
- The extent, mechanism, and consequences of genetic variation, for recombination rate (Q42589609) (← links)
- Pairing, connecting, exchanging, pausing and pulling chromosomes (Q43119215) (← links)
- Global analysis of the meiotic crossover landscape. (Q43196392) (← links)
- An unpaired mouse centromere passes consistently through male meiosis and does not significantly compromise spermatogenesis. (Q47394625) (← links)