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M S Pollack

Showing results (131-140 of 145) with videos related to

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American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
Human Immunology|July 1, 1980
Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locusZ Laron, M S Pollack, R Zamir, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 18, 2002
Phase II study of a moderate-intensity preparative regimen with allogeneic peripheral blood stem cell transplantation for hematologic diseases: the Texas Transplant Consortium experienceP J Shaughnessy, D Ornstein, D Ririe, et al.
American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.
Transplantation Proceedings|February 1, 1993
Degree of HLA mismatch as a predictor of death from allograft arteriopathy after heart transplantB Cocanougher, C M Ballantyne, M S Pollack, et al.
Lancet (London, England)|May 26, 1979
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typingM S Pollack, D Maurer, L S Levine, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Genotyping steroid 21-hydroxylase deficiency: hormonal reference dataM I New, F Lorenzen, A J Lerner, et al.
Annals of the New York Academy of Sciences|January 1, 1984
Generalized lymphadenopathy in homosexual men: an update of the New York experienceC E Metroka, S Cunningham-Rundles, M Krim, et al.
The New England Journal of Medicine|May 2, 1985
Epstein-Barr virus-associated B-cell proliferations of diverse clonal origins after bone marrow transplantation in a 12-year-old patient with severe combined immunodeficiencyW T Shearer, J Ritz, M J Finegold, et al.
Transplantation Proceedings|December 1, 1979
HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type)M S Pollack, D Maurer, L S Levine, et al.
Pageof 15

Showing results (131-140 of 145) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
Human Immunology|July 1, 1980
Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locusZ Laron, M S Pollack, R Zamir, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|September 18, 2002
Phase II study of a moderate-intensity preparative regimen with allogeneic peripheral blood stem cell transplantation for hematologic diseases: the Texas Transplant Consortium experienceP J Shaughnessy, D Ornstein, D Ririe, et al.
American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.
Transplantation Proceedings|February 1, 1993
Degree of HLA mismatch as a predictor of death from allograft arteriopathy after heart transplantB Cocanougher, C M Ballantyne, M S Pollack, et al.
Lancet (London, England)|May 26, 1979
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typingM S Pollack, D Maurer, L S Levine, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Genotyping steroid 21-hydroxylase deficiency: hormonal reference dataM I New, F Lorenzen, A J Lerner, et al.
Annals of the New York Academy of Sciences|January 1, 1984
Generalized lymphadenopathy in homosexual men: an update of the New York experienceC E Metroka, S Cunningham-Rundles, M Krim, et al.
The New England Journal of Medicine|May 2, 1985
Epstein-Barr virus-associated B-cell proliferations of diverse clonal origins after bone marrow transplantation in a 12-year-old patient with severe combined immunodeficiencyW T Shearer, J Ritz, M J Finegold, et al.
Transplantation Proceedings|December 1, 1979
HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type)M S Pollack, D Maurer, L S Levine, et al.
Pageof 15