(Q33331461)

25 July 2017

title

Wiskott Aldrich syndrome presenting as congenital thrombocytopenia (English)

1 reference

25 July 2017

main subject

Wiskott-Aldrich syndrome

0 references

0 references

1 reference

Lawson SE

1

1 reference

25 July 2017

Thompson L

series ordinal

2

1 reference

25 July 2017

Williams MD

series ordinal

3

1 reference

25 July 2017

publication date

1 December 1999

1 reference

International Journal of Laboratory Hematology

25 July 2017

published in

1 reference

25 July 2017

volume

21

1 reference

25 July 2017

issue

6

1 reference

25 July 2017

page(s)

397-399

1 reference

Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype

25 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2257.1999.00273.X

Crossref

reference URL

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2257.1999.00273.X

Crossref

reference URL

Familial idiopathic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2257.1999.00273.X

Crossref

reference URL

10.1046/J.1365-2257.1999.00273.X

21 January 2018

Identifiers

DOI

1 reference

25 July 2017

1 reference