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Molecular Genetics and Metabolism|March 13, 2001
Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiencyC W Lam, W Arlt, C K Chan, et al.The Journal of Clinical Endocrinology and Metabolism|January 1, 1995
Prenatal diagnosis of congenital lipoid adrenal hyperplasiaP Saenger, Z Klonari, S M Black, et al.The Journal of Clinical Investigation|February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasiaY Morel, J André, B Uring-Lambert, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's diseaseD J Devoe, W L Miller, F A Conte, et al.The New England Journal of Medicine|October 20, 2001
A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiencyJ Schalkwijk, M C Zweers, P M Steijlen, et al.Proceedings of the National Academy of Sciences of the United States of America|May 23, 1995
Human steroidogenic acute regulatory protein: functional activity in COS-1 cells, tissue-specific expression, and mapping of the structural gene to 8p11.2 and a pseudogene to chromosome 13T Sugawara, J A Holt, D Driscoll, et al.Biology of Reproduction|December 1, 1995
Isolation of nine different biologically and immunologically active molecular variants of bovine follicular inhibinT E Good, P S Weber, J L Ireland, et al.Advances in Prostaglandin and Thromboxane Research|January 1, 1980
Synthesis and biological activity of 9-deoxo-9-methylene and related prostaglandinsG L Bundy, F A Kimball, A Robert, et al.The Journal of Family Practice|May 23, 1998
Illuminating the 'black box'. A description of 4454 patient visits to 138 family physiciansK C Stange, S J Zyzanski, C R Jaén, et al.Pageof 28