(Q33357787)

26 July 2017

Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation (English)

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Xavier Estivill i Pallejà

26 July 2017

Wiskott-Aldrich syndrome

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author

6

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26 July 2017

Nuria Andreu

1

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Luis Martinez-Lostao

object named as

Luis Martinez-Lostao

3

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author name string

Núria Pujol-Moix

2

1 reference

26 July 2017

Marta Oset

4

1 reference

26 July 2017

Eduardo Muñiz-Diaz

5

1 reference

26 July 2017

Victor Volpini

7

1 reference

26 July 2017

Cristina Fillat

8

1 reference

26 July 2017

1 November 2003

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Blood Cells, Molecules and Diseases

26 July 2017

1 reference

26 July 2017

31

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26 July 2017

3

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26 July 2017

332-337

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Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

26 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

WASp in immune-system organization and function

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Two sisters with clinical diagnosis of Wiskott-Aldrich syndrome: is the condition in the family autosomal recessive?

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Random X chromosome inactivation in a female with a variant of Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

X-linked Wiskott-Aldrich syndrome in a girl

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Wiskott-Aldrich syndrome in a female

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

X-linked thrombocytopenia in a girl

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Age- and tissue-specific variation of X chromosome inactivation ratios in normal women

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

X Inactivation in Females with X-Linked Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

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://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Detection of lymphocytes and granulocytes expressing the mutant WASP message in carriers of Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

A defect in hematopoietic stem cell migration explains the nonrandom X-chromosome inactivation in carriers of Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Immune Deficiency State in a Girl with Eczema and Low Serum IgM: Possible Female Variant of Wiskott-Aldrich Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Wiskott-Aldrich syndrome in two sisters

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1079-9796%2803%2900168-2

7 January 2021

10.1016/S1079-9796(03)00168-2

Identifiers

DOI

1 reference

26 July 2017

1 reference