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Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction (Q69374429)

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scientific article published on 01 October 1989

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English	Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction	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:2571560%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2571560%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Wiskott-Aldrich syndrome

1 reference

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author name string

W L Greer

1

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Europe PubMed Central

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1 October 2019

M M Mahtani

2

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Europe PubMed Central

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1 October 2019

P C Kwong

3

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1 October 2019

L A Rubin

4

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1 October 2019

M Peacocke

5

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1 October 2019

H F Willard

6

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1 October 2019

K A Siminovitch

7

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Europe PubMed Central

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1 October 2019

publication date

1 October 1989

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1 October 2019

language of work or name

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1 October 2019

83

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1 October 2019

3

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1 October 2019

227-230

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1 October 2019

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A primary genetic map of the pericentromeric region of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome-specific organization of human alpha satellite DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome-specific subfamilies within human alphoid repetitive DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wiskott-Aldrich syndrome: studies of lymphocytes, granulocytes, and platelets

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective lymphocyte transformation and delayed hypersensitivity in Wiskott-Aldrich syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp

1 reference

https://pubmed.ncbi.nlm.nih.gov/2571560

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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