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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.
Preventive Veterinary Medicine|October 26, 1999
Public preferences regarding rabies-prevention policies in the UKM Cox, E B Barbier, P C White, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1986
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B proteinP A Donohoue, C van Dop, R H McLean, et al.
Thrombosis and Haemostasis|August 26, 2000
Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factorL Hilbert, P V Jenkins, C Gaucher, et al.
British Journal of Haematology|November 25, 2000
The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophiliaK J Pasi, C A Sabin, P V Jenkins, et al.
International Journal of Obstetric Anesthesia|July 16, 2022
A description of the coagulopathy characteristics in amniotic fluid embolism: a case reportC Oliver, J Freyer, M Murdoch, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|November 27, 2018
Treatment Experiences, Information Needs, Pain and Quality of Life in Men with Metastatic Castrate-resistant Prostate Cancer: Results from the EXTREQOL StudyV Jenkins, I Solis-Trapala, H Payne, et al.
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