Skip to content

Opening book details…

About this Medicine article

Deletion Hybrid Genes, due to Unequal Crossing Over between CYP11B1 (11β-Hydroxylase) and CYP11B2 (Aldosterone Synthase) Cause Steroid 11β-Hydroxylase Deficiency and Congenital Adrenal Hyperplasia 1 by Portrat, Stephanie; Mulatero, Paolo; Curnow, Kathleen M.; Chaussain, Jean-Louis; Morel, Yves; Pascoe, Leigh is a Medicine article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Medicine.

Author
Portrat, Stephanie; Mulatero, Paolo; Curnow, Kathleen M.; Chaussain, Jean-Louis; Morel, Yves; Pascoe, Leigh
Publisher
Endocrine Society; The Endocrine Society; Oxford University Press (ISSN 0021-972X)
Published
2001
Language
EN
Field
Medicine (Health Sciences)

More by Portrat, Stephanie; Mulatero, Paolo; Curnow, Kathleen M.; Chaussain, Jean-Louis; Morel, Yves; Pascoe, Leigh

Browse all works by Portrat, Stephanie; Mulatero, Paolo; Curnow, Kathleen M.; Chaussain, Jean-Louis; Morel, Yves; Pascoe, Leigh