(Q33373197)

English

Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus

scientific article published on May 1, 1991

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scholarly article

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Europe PubMed Central

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17 September 2019

Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1709069%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

Wiskott-Aldrich syndrome

0 references

dosage compensation

1 reference

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4 November 2022

author name string

Mollee-Versteegde IF

5

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17 September 2019

R. W. Hendriks

1

1 reference

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4 November 2022

M. De Weers

2

1 reference

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4 November 2022

R. G. Mensink

3

1 reference

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4 November 2022

M. E. Kraakman

4

1 reference

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4 November 2022

I. F. Mollee-Versteegde

5

1 reference

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4 November 2022

A. J. Veerman

6

0000-0002-9309-301X

1 reference

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4 November 2022

L. A. Sandkuyl

7

1 reference

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4 November 2022

R. K. Schuurman

8

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4 November 2022

language of work or name

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4 November 2022

publication date

1 May 1991

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17 September 2019

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1709069/?tool=EBI

online access status

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4 November 2022

Clinical and Experimental Immunology

1 reference

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17 September 2019

84

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17 September 2019

2

1 reference

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17 September 2019

219-222

1 reference

Europe PubMed Central

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17 September 2019

Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

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/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

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/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in the Wiskott Aldrich syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly informative X-chromosome probe, M27 beta, can be used for the determination of tumour clonality

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

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/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

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/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

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/1709069

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/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation and developmental patterns in mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunoglobulin concentrations in sera of normal children: quantitation against an international reference preparation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1709069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1709069

4 November 2022

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1709069%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

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