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Nature Genetics|July 1, 1992
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase geneE Rhéaume, J Simard, Y Morel, et al.
Medical and Pediatric Oncology|February 1, 1997
A childhood fibrolamellar hepatocellular carcinoma with increased aromatase activity and a near triploid karyotypeM A Hany, D R Betts, M Schmugge, et al.
Hormone Research|January 1, 1992
Growth response to recombinant human growth hormone of mammalian cell origin in prepubertal growth hormone-deficient children during the first two years of treatmentP Stubbe, S D Frasier, N Stahnke, et al.
Helvetica Paediatrica Acta|March 1, 1980
The incidence of congenital adrenal hyperplasia in Switzerland--a survey of patients born in 1960 to 1974E A Werder, R E Siebenmann, G Knorr-Mürset, et al.
Hormone Research|January 1, 1991
Gonadal agenesis in a 46,XY female with multiple malformations and positive testing for the sex-determining region of the Y chromosomeW Sorgo, L Gortner, P Bartmann, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2000
17alpha-hydroxylase/17,20-lyase deficiency as a model to study enzymatic activity regulation: role of phosphorylationA Biason-Lauber, B Kempken, E Werder, et al.
The New England Journal of Medicine|October 26, 1978
Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage groupL S Levine, M Zachmann, M I New, et al.
Journal of Medical Genetics|December 1, 1995
Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome paintingA Schinzel, I Lorda-Sanchez, F Binkert, et al.
British Medical Journal|March 31, 1973
Familial occurrence of persistent Mullerian structures in otherwise normal malesC G Brook, H Wagner, M Zachmann, et al.
Clinical Endocrinology|March 5, 2002
Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complicationsJ Woelfle, W Hoepffner, W G Sippell, et al.
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