N. Kalintchenko

Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis.

V. Prassolov, J. Grötzinger, W. Sippell, 2006, The Journal of clinical endocrinology and metabolism.

A potential rearrangement between CYP19 and TRPM7 genes on chromosome 15q21.2 as a cause of aromatase excess syndrome.

A. Polyakov, V. Peterkova, I. Dedov, 2005, The Journal of clinical endocrinology and metabolism.

Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene

L. Baumbach, V. Peterkova, A. Tiulpakov, 1999 .

Inhibition of Corticotrophin‐Releasing Hormone Transcription by Inducible cAMP‐Early Repressor in the Hypothalamic Cell Line, 4B

P. Sassone-Corsi, G. Aguilera, P. Sassone‐Corsi, 2006, Journal of neuroendocrinology.