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European Journal of Pediatrics
|
November 1, 2001
Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient children
E de Vries, J G Noordzij, T W Kuijpers, et al.
European Journal of Pediatrics
|
January 25, 2002
Reviewing Omenn syndrome
K Aleman, J G Noordzij, R de Groot, et al.
The New England Journal of Medicine
|
October 6, 2001
Development of type 1 diabetes despite severe hereditary B-cell deficiency
S Martin, D Wolf-Eichbaum, G Duinkerken, et al.
Blood
|
July 13, 2000
N-terminal truncated human RAG1 proteins can direct T-cell receptor but not immunoglobulin gene rearrangements
J G Noordzij, N S Verkaik, N G Hartwig, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 10, 2004
[Widely divergent clinical phenotype of x-linked agammaglobulinemia in two cousins]
A G Jansen, J G Noordzij, A H Bröcker-Vriends, et al.
Blood
|
September 15, 1999
The 78C --> T (T254M) XHIM mutation: lack of a tight phenotype-genotype relationship
E de Vries, J G Noordzij, E G Davies, et al.
Archives of Disease in Childhood
|
February 20, 2009
Ataxia-telangiectasia patients presenting with hyper-IgM syndrome
J G Noordzij, N M Wulffraat, A Haraldsson, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
Leukemia
|
December 16, 2006
Human T-cell lines with well-defined T-cell receptor gene rearrangements as controls for the BIOMED-2 multiplex polymerase chain reaction tubes
Y Sandberg, B Verhaaf, E J van Gastel-Mol, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
European Journal of Pediatrics
|
November 1, 2001
Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient children
E de Vries, J G Noordzij, T W Kuijpers, et al.
European Journal of Pediatrics
|
January 25, 2002
Reviewing Omenn syndrome
K Aleman, J G Noordzij, R de Groot, et al.
The New England Journal of Medicine
|
October 6, 2001
Development of type 1 diabetes despite severe hereditary B-cell deficiency
S Martin, D Wolf-Eichbaum, G Duinkerken, et al.
Blood
|
July 13, 2000
N-terminal truncated human RAG1 proteins can direct T-cell receptor but not immunoglobulin gene rearrangements
J G Noordzij, N S Verkaik, N G Hartwig, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 10, 2004
[Widely divergent clinical phenotype of x-linked agammaglobulinemia in two cousins]
A G Jansen, J G Noordzij, A H Bröcker-Vriends, et al.
Blood
|
September 15, 1999
The 78C --> T (T254M) XHIM mutation: lack of a tight phenotype-genotype relationship
E de Vries, J G Noordzij, E G Davies, et al.
Archives of Disease in Childhood
|
February 20, 2009
Ataxia-telangiectasia patients presenting with hyper-IgM syndrome
J G Noordzij, N M Wulffraat, A Haraldsson, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
Leukemia
|
December 16, 2006
Human T-cell lines with well-defined T-cell receptor gene rearrangements as controls for the BIOMED-2 multiplex polymerase chain reaction tubes
Y Sandberg, B Verhaaf, E J van Gastel-Mol, et al.
Page
of 1