Trisomy 21: association between reduced recombination and nondisjunction.
about
Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes.Multipoint estimation of genetic maps for human trisomies with one parent or other partial dataSeasonal variation in the prevalence of Down syndrome at birth: a reviewTroX: a new method to learn about the genesis of aneuploidy from trisomic products of conception.SNaPshot Assay in Quantitative Detection of Allelic Nondisjunction in Down Syndrome.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.Statistical analysis of half-tetradsDetection of nondisjunction and recombination in meiotic and postmeiotic cells from XYSxr [XY,Tp(Y)1Ct] mice using multicolor fluorescence in situ hybridization.Molecular studies of trisomy 18Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.Nondisjunction of chromosome 15: origin and recombinationComparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.DNA polymorphism analysis in families with recurrence of free trisomy 21.Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.First-meiotic-division nondisjunction in human oocytes.Is disomic homozygosity at the APECED locus the cause of increased autoimmunity in Down's syndrome?Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction.Cytogenetic and molecular studies of Down syndrome individuals with leukemia.A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction.Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation.Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphismsCombined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births.Methods for genetic linkage analysis using trisomies.Correction of the evaluation of recombination in meiosis I and II nondisjunction in trisomy 21.Nondisjunction versus nonconjunction.Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.
P2860
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P2860
Trisomy 21: association between reduced recombination and nondisjunction.
description
1991 nî lūn-bûn
@nan
1991 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Trisomy 21: association between reduced recombination and nondisjunction.
@ast
Trisomy 21: association between reduced recombination and nondisjunction.
@en
type
label
Trisomy 21: association between reduced recombination and nondisjunction.
@ast
Trisomy 21: association between reduced recombination and nondisjunction.
@en
prefLabel
Trisomy 21: association between reduced recombination and nondisjunction.
@ast
Trisomy 21: association between reduced recombination and nondisjunction.
@en
P2093
P2860
P1476
Trisomy 21: association between reduced recombination and nondisjunction
@en
P2093
A E Cockwell
C Phillips
M Grantham
P A Jacobs
R D Blackston
S B Freeman
S L Sherman
P2860
P304
P407
P577
1991-09-01T00:00:00Z