(Q47642533)

4 February 2018

title

A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies (English)

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4 February 2018

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Wengler GS

1

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4 February 2018

Parolini O

2

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4 February 2018

Fiorini M

3

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4 February 2018

Mella P

4

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4 February 2018

Smith H

5

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4 February 2018

Ugazio AG

6

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4 February 2018

Notarangelo LD

7

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4 February 2018

language of work or name

English

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publication date

1 January 1997

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4 February 2018

published in

Life Sciences

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4 February 2018

volume

61

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4 February 2018

issue

14

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4 February 2018

page(s)

1405-1411

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4 February 2018

Gene action in the X-chromosome of the mouse (Mus musculus L.)

cites work

1 reference

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.

7 January 2021

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Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Carrier detection in typical and atypical X-linked agammaglobulinemia

7 January 2021

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Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytes

7 January 2021

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Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans

7 January 2021

1 reference

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The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0024-3205%2897%2900686-3

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

7 January 2021

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10.1016/S0024-3205(97)00686-3

7 January 2021

Identifiers

DOI

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4 February 2018

1 reference

4 February 2018