Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21

scientific article

Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21 is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode1988PNAS...85.4794S
P356DOI10.1073/PNAS.85.13.4794
P932PMC publication ID280522
P698PubMed publication ID2898783
P5875ResearchGate publication ID20257042

P50authorJames F. GusellaQ1602688
P2093author name stringPapas TS
Bricarelli FD
Perroni L
Sacchi N
P2860cites workThe ets sequence from the transforming gene of avian erythroblastosis virus, E26, has unique domains on human chromosomes 11 and 21: both loci are transcriptionally activeQ24609161
Isolation of polymorphic DNA segments from human chromosome 21.Q35559585
Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21Q37688575
The genetic control of meiosisQ52431584
Meiosis-specific transcripts of a DNA component replicated during chromosome pairing: Homology across the phylogenetic spectrumQ61981716
P433issue13
P407language of work or nameEnglishQ1860
P304page(s)4794-4798
P577publication date1988-07-01
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleLack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on chromosome 21
P478volume85

Reverse relations

cites work (P2860)
Q35881410Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction
Q43553889Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis
Q68328473Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21
Q31159522Down syndrome and chromosome 21 abnormalities in leukaemia
Q44650244High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms
Q33655836Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease
Q37685279Molecular and functional characterization of the promoter of ETS2, the human c-ets-2 gene
Q34311468c-ets-2 protooncogene has mitogenic and oncogenic activity