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Recent Progress in Hormone Research|January 1, 1994
Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridizationP W Speiser, P C White, J Dupont, et al.
The Journal of Pediatrics|July 13, 2000
Time course of recovery of adrenal function in children treated for leukemiaE I Felner, M T Thompson, A F Ratliff, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Nucleotide sequence analysis of murine 21-hydroxylase genes: mutations affecting gene expressionD D Chaplin, L J Galbraith, J G Seidman, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 30, 2012
ARIX: a randomised trial of acupuncture v oral care sessions in patients with chronic xerostomia following treatment of head and neck cancerR Simcock, L Fallowfield, K Monson, et al.
British Journal of Haematology|February 26, 2000
Type 1 von Willebrand disease - a clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding historyI C Nitu-Whalley, C A Lee, A Griffioen, et al.
Thrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.
Breast Cancer Research and Treatment|January 4, 2022
IMPARTER, Phase 1 of an intervention to improve patients' understanding of gene expression profiling tests in breast cancerL J Fallowfield, D Farewell, H Jones, et al.
American Journal of Orthopedics (Belle Mead, N.J.)|July 28, 2012
Traumatic C4-C5 unilateral facet dislocation with posterior disc herniation above a prior anterior fusionNoah M Raizman, Warren D Yu, Matthew V Jenkins, et al.
Endocrine Research|February 24, 2001
Genotype-phenotype correlations of mutations and polymorphisms in HSD11B2, the gene encoding the kidney isozyme of 11beta-hydroxysteroid dehydrogenaseP C White, A K Agarwal, B S Nunez, et al.
Molecular Endocrinology (Baltimore, Md.)|September 8, 2000
Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domainH Nikkila, D R McMillan, B S Nunez, et al.
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