Genetic linkage map of human chromosome 21

scientific article published on 01 August 1988

Genetic linkage map of human chromosome 21 is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0888-7543(88)90143-7
P698PubMed publication ID2906323

P50authorJonathan L HainesQ73570557
James F. GusellaQ1602688
P2093author name stringP C Watkins
C Wong
M R Wallace
P M Conneally
R E Tanzi
N S Wexler
G D Stewart
R Hallewell
P433issue2
P304page(s)129-136
P577publication date1988-08-01
P1433published inGenomicsQ5533503
P1476titleGenetic linkage map of human chromosome 21
P478volume3

Reverse relations

cites work (P2860)
Q24562094A contiguous Not I restriction map of band q22.3 of human chromosome 21
Q35199346A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age
Q30741023A genetic linkage map of human chromosome 9q
Q68293112A molecular genetic approach to the identification of isochromosomes of chromosome 21
Q33917989An interspersed repeated sequence specific for human subtelomeric regions
Q33916503Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions
Q35814879Clustering of multiallele DNA markers near the Huntington's disease gene
Q34294835Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
Q68328473Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21
Q69374432Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping
Q33594855Exclusion of familial dysautonomia from more than 60% of the genome
Q34481619Five polymorphic microsatellite VNTRs on the human X chromosome.
Q30541697Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.
Q41606196Generation of 19 STS markers that can be anchored at specific sites on human chromosome 21.
Q34769174Genetic linkage studies of human neurodegenerative disorders
Q53299482Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.
Q29614956Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection
Q33655836Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease
Q53181217Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.
Q33244565Increased recombination adjacent to the Huntington disease-linked D4S10 marker
Q68039006Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studies
Q35716444Integrating maps of chromosome 21.
Q40452349Isolation and characterization of a human telomere
Q35196469Linkage analysis of familial Alzheimer disease, using chromosome 21 markers
Q24675154Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3
Q24678931Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage
Q52224929Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.
Q33579172Long-range restriction map of the terminal part of the short arm of the human X chromosome
Q70485032Mapping the way ahead
Q69928858Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes
Q35201305Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21
Q53187559Predisposing locus for Alzheimer's disease on chromosome 21.
Q35196918Protocols to establish genotype-phenotype correlations in Down syndrome
Q34595912Random-breakage mapping method applied to human DNA sequences
Q38982671Recent Perspectives on APP, Secretases, Endosomal Pathways and How they Influence Alzheimer's Related Pathological Changes in Down Syndrome
Q41652589Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease
Q57162306Report of the fourth international workshop on human chromosome 21
Q28241772Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
Q67577183Sequence-tagged sites (STSs) for a set of mapped markers on chromosome 21
Q53208536Susceptibility genes for familial Alzheimer's disease on chromosomes 19 and 21: a reality check.
Q38060615Telomere shortening and Alzheimer's disease.
Q35327219The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer's disease
Q40519621The proterminal regions and telomeres of human chromosomes.
Q35196790Trisomy 21: association between reduced recombination and nondisjunction
Q34854001Turnover of amyloid precursor protein family members determines their nuclear signaling capability

Search more.