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M L Markert

Showing results (21-30 of 35) with videos related to

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American Journal of Human Genetics|October 1, 1992
Molecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiencyM R Aust, L G Andrews, M J Barrett, et al.
Clinical Immunology (Orlando, Fla.)|May 5, 1999
Possible extrathymic development of nonfunctional T cells in a patient with complete DiGeorge syndromeH R Collard, A Boeck, T M Mc Laughlin, et al.
Seminars in Hematology|October 1, 1993
Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiencyR H Buckley, S E Schiff, R I Schiff, et al.
The Journal of Pediatrics|February 21, 1998
Complete DiGeorge syndrome: persistence of profound immunodeficiencyM L Markert, D S Hummell, H M Rosenblatt, et al.
The Journal of Pediatrics|March 1, 1997
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infantsR H Buckley, R I Schiff, S E Schiff, et al.
Journal of Clinical Immunology|March 1, 1997
Normalization of the peripheral blood T cell receptor V beta repertoire after cultured postnatal human thymic transplantation in DiGeorge syndromeC M Davis, T M McLaughlin, T J Watson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1987
Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiencyM L Markert, M S Hershfield, D A Wiginton, et al.
Human Mutation|January 1, 1997
Mutations in purine nucleoside phosphorylase deficiencyM L Markert, B D Finkel, T M McLaughlin, et al.
The New England Journal of Medicine|March 5, 1987
Treatment of adenosine deaminase deficiency with polyethylene glycol-modified adenosine deaminaseM S Hershfield, R H Buckley, M L Greenberg, et al.
AIDS Research and Human Retroviruses|January 10, 2002
Thymopoiesis in HIV-infected adults after highly active antiretroviral therapyM L Markert, A P Alvarez-McLeod, G D Sempowski, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|October 1, 1992
Molecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiencyM R Aust, L G Andrews, M J Barrett, et al.
Clinical Immunology (Orlando, Fla.)|May 5, 1999
Possible extrathymic development of nonfunctional T cells in a patient with complete DiGeorge syndromeH R Collard, A Boeck, T M Mc Laughlin, et al.
Seminars in Hematology|October 1, 1993
Haploidentical bone marrow stem cell transplantation in human severe combined immunodeficiencyR H Buckley, S E Schiff, R I Schiff, et al.
The Journal of Pediatrics|February 21, 1998
Complete DiGeorge syndrome: persistence of profound immunodeficiencyM L Markert, D S Hummell, H M Rosenblatt, et al.
The Journal of Pediatrics|March 1, 1997
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infantsR H Buckley, R I Schiff, S E Schiff, et al.
Journal of Clinical Immunology|March 1, 1997
Normalization of the peripheral blood T cell receptor V beta repertoire after cultured postnatal human thymic transplantation in DiGeorge syndromeC M Davis, T M McLaughlin, T J Watson, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1987
Identification of a deletion in the adenosine deaminase gene in a child with severe combined immunodeficiencyM L Markert, M S Hershfield, D A Wiginton, et al.
Human Mutation|January 1, 1997
Mutations in purine nucleoside phosphorylase deficiencyM L Markert, B D Finkel, T M McLaughlin, et al.
The New England Journal of Medicine|March 5, 1987
Treatment of adenosine deaminase deficiency with polyethylene glycol-modified adenosine deaminaseM S Hershfield, R H Buckley, M L Greenberg, et al.
AIDS Research and Human Retroviruses|January 10, 2002
Thymopoiesis in HIV-infected adults after highly active antiretroviral therapyM L Markert, A P Alvarez-McLeod, G D Sempowski, et al.
Pageof 4