Results 151 to 160 of about 76,273 (258)

Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.

open access: yesJournal of Medical Genetics, 1986
G. Rumsby   +4 more
semanticscholar   +1 more source

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.

open access: yesProceedings of the National Academy of Sciences of the United States of America, 1988
M. Amor   +4 more
semanticscholar   +1 more source

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.

open access: yesProceedings of the National Academy of Sciences of the United States of America, 1989
Y. Morel   +3 more
semanticscholar   +1 more source

Neurosteroids in pain management: A new perspective on an old player [PDF]

open access: yes, 2018
Covey, Douglas F   +3 more
core   +2 more sources

Uncontrolled hypertension in siblings: an unsuspected diagnosis. [PDF]

open access: yesAJOG Glob Rep
Aleem S   +3 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy