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P C White

Showing results (141-150 of 183) with videos related to

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Advances in Experimental Medicine and Biology|April 30, 1998
Detailed analysis of human cathepsin E prime region specificityM Bukhtiyarova, C Rao-Naik, P J Tatnell, et al.
Human Genetics|April 1, 1994
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.
Journal of Dental Research|October 8, 2015
Neutrophil Extracellular Traps in Periodontitis: A Web of IntrigueP C White, I J Chicca, P R Cooper, et al.
Journal of Internal Medicine|August 11, 1998
Associations between aldosterone synthase gene polymorphism and the adrenocortical function in malesA Hautanena, L Lankinen, M Kupari, et al.
Immunogenetics|January 1, 1992
Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7A Selvakumar, B K Mohanraj, R L Eddy, et al.
Human Molecular Genetics|December 1, 1996
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.
Nature|November 5, 1984
Two steroid 21-hydroxylase genes are located in the murine S regionP C White, D D Chaplin, J H Weis, et al.
Human Genetics|March 1, 1992
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, M I New, G M Tannin, et al.
American Journal of Human Genetics|January 1, 1991
Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiencyE Mornet, P Crété, F Kuttenn, et al.
Endocrinology|October 3, 2000
Transcriptional regulation of human 11beta-hydroxylase (hCYP11B1)X L Wang, M Bassett, Y Zhang, et al.
Pageof 19

Showing results (141-150 of 183) with videos related to

Sort By:
Pageof 19
Advances in Experimental Medicine and Biology|April 30, 1998
Detailed analysis of human cathepsin E prime region specificityM Bukhtiyarova, C Rao-Naik, P J Tatnell, et al.
Human Genetics|April 1, 1994
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.
Journal of Dental Research|October 8, 2015
Neutrophil Extracellular Traps in Periodontitis: A Web of IntrigueP C White, I J Chicca, P R Cooper, et al.
Journal of Internal Medicine|August 11, 1998
Associations between aldosterone synthase gene polymorphism and the adrenocortical function in malesA Hautanena, L Lankinen, M Kupari, et al.
Immunogenetics|January 1, 1992
Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7A Selvakumar, B K Mohanraj, R L Eddy, et al.
Human Molecular Genetics|December 1, 1996
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigreesD J Day, P W Speiser, E Schulze, et al.
Nature|November 5, 1984
Two steroid 21-hydroxylase genes are located in the murine S regionP C White, D D Chaplin, J H Weis, et al.
Human Genetics|March 1, 1992
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, M I New, G M Tannin, et al.
American Journal of Human Genetics|January 1, 1991
Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiencyE Mornet, P Crété, F Kuttenn, et al.
Endocrinology|October 3, 2000
Transcriptional regulation of human 11beta-hydroxylase (hCYP11B1)X L Wang, M Bassett, Y Zhang, et al.
Pageof 19