Pages that link to "Q41355917"

The following pages link to Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome (Q41355917):

Displaying 50 items.

• Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes (Q24530701) (← links)
• Association between maternal age and meiotic recombination for trisomy 21. (Q24530760) (← links)
• Risk factors for Down syndrome (Q30245584) (← links)
• Multipoint estimation of genetic maps for human trisomies with one parent or other partial data (Q30587139) (← links)
• Down syndrome and chromosome 21 abnormalities in leukaemia (Q31159522) (← links)
• Broad-scale recombination patterns underlying proper disjunction in humans (Q33504545) (← links)
• High-resolution sex-specific linkage maps of the mouse reveal polarized distribution of crossovers in male germline (Q33575874) (← links)
• Molecular studies of non-disjunction in trisomy 16. (Q33596635) (← links)
• Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data (Q33643852) (← links)
• An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction (Q33753775) (← links)
• Down syndrome: genetic recombination and the origin of the extra chromosome 21. (Q33874300) (← links)
• The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project (Q34007112) (← links)
• The management of neoplastic disorders of haematopoiesis in children with Down's syndrome (Q34039933) (← links)
• Rare etiology of autosomal recessive disease in a child with noncarrier parents (Q34142703) (← links)
• Etiology of nondisjunction in humans (Q34313631) (← links)
• Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin. (Q34387428) (← 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)
• Fine-scale mapping of meiotic recombination in Asians (Q34627535) (← links)
• Genetic anomalies in mammalian germ cells and their significance for human reproductive and developmental risk (Q34848205) (← links)
• Detection of nondisjunction and recombination in meiotic and postmeiotic cells from XYSxr [XY,Tp(Y)1Ct] mice using multicolor fluorescence in situ hybridization (Q34981455) (← links)
• Cytological studies of human meiosis: sex-specific differences in recombination originate at, or prior to, establishment of double-strand breaks (Q35078534) (← links)
• Maternal age effect: The enigma of Down syndrome and other trisomic conditions (Q35148541) (← links)
• Molecular studies of trisomy 18 (Q35194706) (← links)
• Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect. (Q35194845) (← links)
• Nondisjunction of chromosome 15: origin and recombination (Q35195059) (← links)
• No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements (Q35195124) (← links)
• Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome (Q35195816) (← links)
• Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome (Q35195831) (← links)
• DNA polymorphism analysis in families with recurrence of free trisomy 21 (Q35196148) (← links)
• Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal (Q35196747) (← links)
• Trisomy 21: association between reduced recombination and nondisjunction (Q35196790) (← links)
• XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region (Q35197098) (← links)
• The parental origin of the extra X chromosome in 47,XXX females. (Q35197998) (← links)
• Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers (Q35198328) (← links)
• Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations (Q35198592) (← links)
• The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms (Q35199335) (← links)
• A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age (Q35199346) (← links)
• On the origin of chromosome anomaly (Q35245848) (← links)
• The probability of detecting the origin of nondisjunction of autosomal trisomies (Q35248326) (← links)
• Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction (Q35643249) (← 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)
• Down syndrome: parental origin, recombination, and maternal age. (Q35693739) (← links)
• The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects (Q35778122) (← links)
• Meiotic origins of maternal age-related aneuploidy (Q35855863) (← links)
• A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis (Q36723618) (← links)
• The effect of parental age on the presence of de novo mutations - Lessons from neurofibromatosis type I. (Q37101242) (← links)
• Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction (Q37219944) (← links)
• Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. (Q37406436) (← links)
• Recent advance in our understanding of the molecular nature of chromosomal abnormalities. (Q37448159) (← links)
• Two-parameter characterization of chromosome-scale recombination rate. (Q37471856) (← links)