Search research articles
Contact Us
Filters
Showing results (21-30 of 99) with videos related to
Page
of 10
Sort By:
Human Genetics
|
May 1, 1997
Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilization
J M Puck, L Middelton, A E Pepper
Human Molecular Genetics
|
September 1, 1995
Intronic point mutation in the IL2RG gene causing X-linked severe combined immunodeficiency
C Tassara, A E Pepper, J M Puck
The New England Journal of Medicine
|
May 15, 1997
The Canale-Smith syndrome
S E Straus, M Lenardo, J M Puck
The New England Journal of Medicine
|
April 16, 1998
The interleukin-4 receptor variant Q576R in hyper-IgE syndrome
B Grimbacher, S M Holland, J M Puck
American Journal of Human Genetics
|
July 1, 1993
Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13
J M Puck, M E Conley, L C Bailey
Genomics
|
January 1, 1993
Twelve new polymorphic microsatellites on human chromosome 22
J C Porter, K T Ram, J M Puck
Cellular Immunology
|
September 1, 1982
Bromodeoxyuridine and light treatment enhances responsiveness of pokeweed mitogen-stimulated human lymphocytes to autologous and allogeneic determinants
J M Puck, S L Abramson, R R Rich
The Journal of Clinical Investigation
|
May 1, 1987
Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation
J M Puck, R L Nussbaum, M E Conley
The Journal of Experimental Medicine
|
October 1, 1981
Antigen presentation to human T lymphocytes. I. Different requirements for stimulation by hapten-modified cells vs. cell sonicates
S L Abramson, J M Puck, R R Rich
Nucleic Acids Research
|
September 25, 1989
RFLPs in human X-linked PGK1: a new probe for the PstI RFLP demonstrates strong linkage disequilibrium with the BgII RFLP
D L Smead, R L Nussbaum, J M Puck
Page
of 10
Search research articles
Search
Showing results (21-30 of 99) with videos related to
Sort By:
Page
of 10
Human Genetics
|
May 1, 1997
Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilization
J M Puck, L Middelton, A E Pepper
Human Molecular Genetics
|
September 1, 1995
Intronic point mutation in the IL2RG gene causing X-linked severe combined immunodeficiency
C Tassara, A E Pepper, J M Puck
The New England Journal of Medicine
|
May 15, 1997
The Canale-Smith syndrome
S E Straus, M Lenardo, J M Puck
The New England Journal of Medicine
|
April 16, 1998
The interleukin-4 receptor variant Q576R in hyper-IgE syndrome
B Grimbacher, S M Holland, J M Puck
American Journal of Human Genetics
|
July 1, 1993
Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13
J M Puck, M E Conley, L C Bailey
Genomics
|
January 1, 1993
Twelve new polymorphic microsatellites on human chromosome 22
J C Porter, K T Ram, J M Puck
Cellular Immunology
|
September 1, 1982
Bromodeoxyuridine and light treatment enhances responsiveness of pokeweed mitogen-stimulated human lymphocytes to autologous and allogeneic determinants
J M Puck, S L Abramson, R R Rich
The Journal of Clinical Investigation
|
May 1, 1987
Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation
J M Puck, R L Nussbaum, M E Conley
The Journal of Experimental Medicine
|
October 1, 1981
Antigen presentation to human T lymphocytes. I. Different requirements for stimulation by hapten-modified cells vs. cell sonicates
S L Abramson, J M Puck, R R Rich
Nucleic Acids Research
|
September 25, 1989
RFLPs in human X-linked PGK1: a new probe for the PstI RFLP demonstrates strong linkage disequilibrium with the BgII RFLP
D L Smead, R L Nussbaum, J M Puck
Page
of 10