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Human Heredity|April 3, 1999
Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiencyT A Bachega, A E Billerbeck, G Madureira, et al.Nature Genetics|May 1, 1994
Male pseudohermaphroditism caused by mutations of testicular 17 beta-hydroxysteroid dehydrogenase 3W M Geissler, D L Davis, L Wu, et al.Revista Da Sociedade Brasileira De Medicina Tropical|September 1, 1996
[Treatment of american cutaneous leishmaniasis, with lesions in the mucosa, using pentamidine isethionate]V S Amato, J G de Paula, R Imamura, et al.International Endodontic Journal|October 10, 2024
Ultrastructural evaluation of adverse effects on dentine formation from systemic fluoride application in an experimental mouse modelMotoki Okamoto, Shohei Yamashita, Melanie Mendonca, et al.The Journal of Clinical Endocrinology and Metabolism|October 16, 1999
Diagnostic value of fluorometric assays in the evaluation of precocious pubertyV N Brito, M C Batista, M F Borges, et al.European Journal of Medical Genetics|June 12, 2010
Usefulness of MLPA in the detection of SHOX deletionsMariana F A Funari, Alexander A L Jorge, Silvia C A L Souza, et al.Brazilian Journal of Otorhinolaryngology|June 21, 2012
Quality of life assessment septoplasty in patients with nasal obstructionThiago Freire Pinto Bezerra, Michael G Stewart, Marco Aurelio Fornazieri, et al.Radiation Research|December 20, 2007
Parthenolide sensitizes cells to X-ray-induced cell killing through inhibition of NF-kappaB and split-dose repairMarc S Mendonca, Helen Chin-Sinex, Jaime Gomez-Millan, et al.Clinical Endocrinology|January 5, 2007
SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variabilityAlexander A L Jorge, Silvia C Souza, Miriam Y Nishi, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 28, 2013
The IRS1 G972R polymorphism and glomerular filtration rate in patients with type 2 diabetes of European ancestrySalvatore De Cosmo, Sabrina Prudente, Olga Lamacchia, et al.Pageof 166