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Medicine|March 1, 1992
Neonatal lupus erythematosus syndrome: analysis of C4 allotypes and C4 genes in 18 familiesR M Watson, J N Scheel, M Petri, 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.
Biochemical and Biophysical Research Communications|February 13, 1987
Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasiaN Jospe, P A Donohoue, C Van Dop, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1993
Alport syndrome: from bedside to genome to bedsideC E Kashtan, A F Michael
The American Journal of Anatomy|February 1, 1990
Expression of novel basement membrane components in the developing human kidney and eyeM M Kleppel, A F Michael
Archives of Pathology & Laboratory Medicine|November 1, 1978
Focal glomerular sclerosis and sarcoidosisS M Lee, A F Michael
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 1, 1983
Retardation of fading and enhancement of intensity of immunofluorescence by p-phenylenediamineJ L Platt, A F Michael
Uremia Investigation|January 1, 1984
Analysis of renal cell populations using monoclonal antibodiesJ L Platt, A F Michael
Kidney International|January 1, 1988
Acute tubulointerstitial nephritis associated with aminonucleoside nephrosisA A Eddy, A F Michael
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