Literature DB >> 4161668

Inherited thrombocytopenia.

M Ata, O D Fisher, C A Holman.   

Abstract

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Year:  1965        PMID: 4161668     DOI: 10.1016/s0140-6736(65)91087-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  5 in total

Review 1.  Genetics of human X-linked immunodeficiency diseases.

Authors:  R W Hendriks; R K Schuurman
Journal:  Clin Exp Immunol       Date:  1991-08       Impact factor: 4.330

2.  Familial idiopathic thrombocytopenic purpura. Raynaud's phenomenon.

Authors:  J P Ellis; H M Clink
Journal:  Proc R Soc Med       Date:  1969-12-12

3.  Immune deficiency state in a girl with eczema and low serum IgM. Possible female variant of Wiskott-Aldrich syndrome.

Authors:  D I Evans; A Holzel
Journal:  Arch Dis Child       Date:  1970-08       Impact factor: 3.791

4.  A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.

Authors:  C P Bennett; A J Barnicoat; F Cotter; Q Wang; C G Mathew
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

5.  X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.

Authors:  G De Saint-Basile; N Schlegel; M Caniglia; F Le Deist; C Kaplan; T Lecompte; F Piller; A Fischer; C Griscelli
Journal:  Ann Hematol       Date:  1991-08       Impact factor: 3.673

  5 in total

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