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The New England Journal of Medicine
|
April 12, 1990
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis
J M Puck, C M Krauss, S M Puck, et al.
Blood
|
May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiency
M E Conley, N B Spinner, B S Emanuel, et al.
Transfusion
|
March 1, 1988
Direct quantitation of IgG subclasses 1, 2, and 3 bound to red cells by Rh1 (D) antibodies
D R Shaw, M E Conley, F J Knox, et al.
The Journal of Experimental Medicine
|
January 31, 1998
Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia
Y Minegishi, E Coustan-Smith, Y H Wang, et al.
Blood
|
September 1, 1992
Atypical Wiskott-Aldrich syndrome in a girl
M E Conley, W C Wang, O Parolini, et al.
Immunogenetics
|
January 1, 1994
The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia
J Rohrer, O Parolini, J W Belmont, et al.
Blood
|
June 15, 1990
Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivation
J M Puck, K A Siminovitch, M Poncz, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 20, 2000
The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease
C F Webb, Y Yamashita, N Ayers, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features
Yanick Joseph Crow, J A Goodship, C Wright, et al.
Immunogenetics
|
October 31, 2001
Variations in the human phospholipase Cgamma2 gene in patients with B-cell defects of unknown etiology
D Wang, E C Boylin, Y Minegishi, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 116) with videos related to
Sort By:
Page
of 12
The New England Journal of Medicine
|
April 12, 1990
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis
J M Puck, C M Krauss, S M Puck, et al.
Blood
|
May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiency
M E Conley, N B Spinner, B S Emanuel, et al.
Transfusion
|
March 1, 1988
Direct quantitation of IgG subclasses 1, 2, and 3 bound to red cells by Rh1 (D) antibodies
D R Shaw, M E Conley, F J Knox, et al.
The Journal of Experimental Medicine
|
January 31, 1998
Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia
Y Minegishi, E Coustan-Smith, Y H Wang, et al.
Blood
|
September 1, 1992
Atypical Wiskott-Aldrich syndrome in a girl
M E Conley, W C Wang, O Parolini, et al.
Immunogenetics
|
January 1, 1994
The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia
J Rohrer, O Parolini, J W Belmont, et al.
Blood
|
June 15, 1990
Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivation
J M Puck, K A Siminovitch, M Poncz, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 20, 2000
The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease
C F Webb, Y Yamashita, N Ayers, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
A newly recognized, likely autosomal recessive syndrome comprising agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis, and other features
Yanick Joseph Crow, J A Goodship, C Wright, et al.
Immunogenetics
|
October 31, 2001
Variations in the human phospholipase Cgamma2 gene in patients with B-cell defects of unknown etiology
D Wang, E C Boylin, Y Minegishi, et al.
Page
of 12