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J G Noordzij

Showing results (1-10 of 9) with videos related to

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European Journal of Pediatrics|November 1, 2001
Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient childrenE de Vries, J G Noordzij, T W Kuijpers, et al.
European Journal of Pediatrics|January 25, 2002
Reviewing Omenn syndromeK 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 deficiencyS 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 rearrangementsJ 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 relationshipE 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 syndromeJ 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 tubesY Sandberg, B Verhaaf, E J van Gastel-Mol, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
European Journal of Pediatrics|November 1, 2001
Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient childrenE de Vries, J G Noordzij, T W Kuijpers, et al.
European Journal of Pediatrics|January 25, 2002
Reviewing Omenn syndromeK 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 deficiencyS 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 rearrangementsJ 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 relationshipE 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 syndromeJ 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 tubesY Sandberg, B Verhaaf, E J van Gastel-Mol, et al.
Pageof 1