Pages that link to "Q72449224"
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The following pages link to Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination (Q72449224):
Displaying 50 items.
- Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes (Q24530701) (← links)
- Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16 (Q24671536) (← links)
- New insights into the generation and role of de novo mutations in health and disease (Q28073446) (← links)
- Prenatal Diagnosis (Q29306683) (← links)
- Multipoint estimation of genetic maps for human trisomies with one parent or other partial data (Q30587139) (← links)
- Multipoint genetic mapping with trisomy data (Q30665451) (← links)
- Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? (Q33681527) (← links)
- Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21. (Q33682320) (← links)
- TroX: a new method to learn about the genesis of aneuploidy from trisomic products of conception (Q33841849) (← links)
- Age-dependent recombination rates in human pedigrees (Q34017511) (← links)
- Quantifying and modeling birth order effects in autism (Q34062417) (← links)
- Rejuvenation of meiotic cohesion in oocytes during prophase I is required for chiasma maintenance and accurate chromosome segregation (Q34165760) (← links)
- Abnormal microRNA expression in Ts65Dn hippocampus and whole blood: contributions to Down syndrome phenotypes (Q34229190) (← links)
- Etiology of nondisjunction in humans (Q34313631) (← links)
- Statistical analysis of half-tetrads (Q34605310) (← 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)
- Molecular analysis of nondisjunction in mice heterozygous for a Robertsonian translocation. (Q34615455) (← links)
- Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities (Q35019247) (← links)
- Understanding mental retardation in Down's syndrome using trisomy 16 mouse models (Q35204307) (← links)
- First-meiotic-division nondisjunction in human oocytes (Q35248934) (← links)
- Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction (Q35643249) (← links)
- Cytogenetic and molecular studies of Down syndrome individuals with leukemia. (Q35643435) (← links)
- A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination (Q35644505) (← links)
- Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. (Q35881553) (← links)
- Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome (Q35882171) (← links)
- Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations (Q36135438) (← links)
- The development of colon innervation in trisomy 16 mice and Hirschsprung's disease. (Q36397307) (← links)
- A fascination with chromosome rescue in uniparental disomy: Mendelian recessive outlaws and imprinting copyrights infringements (Q36488731) (← links)
- Embryo aneuploidy screening for repeated implantation failure and unexplained recurrent miscarriage. (Q36527052) (← links)
- Meiotic recombination at the ends of chromosomes in Saccharomyces cerevisiae. (Q36778028) (← links)
- Heterochromatin-mediated association of achiasmate homologs declines with age when cohesion is compromised (Q37152661) (← links)
- Patterns of meiotic recombination in human fetal oocytes (Q37217307) (← links)
- Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction (Q37219944) (← links)
- Effect of sex, age and genetics on crossover interference in cattle (Q37445187) (← links)
- Recent advance in our understanding of the molecular nature of chromosomal abnormalities. (Q37448159) (← links)
- Enlightenment of yeast mitochondrial homoplasmy: diversified roles of gene conversion (Q37585041) (← links)
- Exchanges are not equally able to enhance meiotic chromosome segregation in yeast (Q37611056) (← links)
- Noninvasive prenatal testing: the future is now. (Q38182095) (← links)
- Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction (Q38478895) (← links)
- Unaltered meiotic chromosome segregation in Drosophila melanogaster raised on a 5% quercetin diet. (Q38550798) (← links)
- Chromosome abnormalities in human beings. (Q40872596) (← links)
- Parental age-related aneuploidy in human germ cells and offspring: a story of past and present (Q40956476) (← links)
- Chiasmata, crossovers, and meiotic chromosome segregation. (Q41625134) (← links)
- Does aneuploidy per se cause developmental abnormalities? (Q41685060) (← links)
- When does maternal age-dependent trisomy 21 arise relative to meiosis? (Q42587521) (← links)
- Premeiotic trisomy 21 in oocytes and Down syndrome: a reply to Zheng and Byers's hypothesis (Q42589477) (← links)
- Methods for genetic linkage analysis using trisomies. (Q42743148) (← links)
- Human female meiosis: new insights into an error-prone process (Q43105072) (← links)