Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping (Q69374432)

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scientific article published on 01 October 1989

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English	Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping	scientific article published on 01 October 1989

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2571564%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping (English)

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Europe PubMed Central

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1 October 2019

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H Meijer

1

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1 October 2019

G J Hamers

2

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1 October 2019

R J Jongbloed

3

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1 October 2019

G P Vaes-Peeters

4

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1 October 2019

R R van der Hulst

5

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1 October 2019

J P Geraedts

6

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1 October 2019

publication date

1 October 1989

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1 October 2019

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1 October 2019

83

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1 October 2019

3

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1 October 2019

280-286

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1 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00285173

0 references

Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

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Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21.

1 reference

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12 December 2020

based on heuristic

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Leukemia and other Cancers, Anomalies and Infections as Causes of Death in Down's Syndrome in the United States during 1976

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

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On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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The biology of Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

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Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Satellite DNA and heterochromatin variants: The case for unequal mitotic crossing over

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

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Reduced recombination rate on chromosomes 21 that have undergone nondisjunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of DNA probes to establish parental origin in Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Oxygen consumption of phagocytizing cells in human leukocyte and granulocyte preparations: a comparative study

1 reference

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12 December 2020

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The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Further studies on bivalent chiasma frequency in human males with normal karyotypes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal age and origin of non-disjunction in trisomy 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage map of human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and chromosomal localization of a cDNA encoding brain amyloid of Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Down's syndrome. Recent trends in the United States

1 reference

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12 December 2020

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Genetic syndromes in man with potential relevance to the pathobiology of aging

1 reference

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The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

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Isolation and regional mapping of DNA sequences unique to human chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RFLPS at the D21S19 locus of human chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of the extra chromosome in Down's Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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