Genotype versus phenotype in families with androgen insensitivity syndrome

Androgen insensitivity syndrome encompasses a wide range of phenotypes, which are caused by numerous different mutations in the AR gene. Detailed information on the genotype/phenotype relationship in androgen insensitivity syndrome is important for sex assignment, treatment of androgen insensitivity syndrome patients, genetic counseling of their families, and insight into the functional domains of the AR. The commonly accepted concept of dependence on fetal androgens of the development of Wolffian ducts was studied in complete androgen insensitivity syndrome (CAIS) patients. In a nationwide su... Mehr ...

Verfasser: Boehmer, A.L.M. (Annemie)
Oostdijk, W. (Wilma)
Brüggenwirth, H.T. (Hennie)
Assendelft, C. van
Drop, S.L.S. (Stenvert)
Otten, B.J. (Barto)
Verleun-Mooijman, M.C.
Niermeijer, M.F. (Martinus)
Vroede, M.A. de
Brunner, H.G. (Han)
Rouwé, C.W. (Catrienus)
Kwast, Th.H. (Theo) van der
Waelkens, J.J.J. (Johan)
Kleijer, W.J. (Wim)
Dokumenttyp: Artikel
Erscheinungsdatum: 2001
Schlagwörter: Adolescent / Adult / Androgen-Insensitivity Syndrome/epidemiology/*genetics/pathology / Child / Preschool / Comparative Study / DNA/genetics / Electrophoresis / Polyacrylamide Gel / Female / Gene Frequency / Genotype / Humans / Immunohistochemistry / Infant / Male / Netherlands/epidemiology / Pedigree / Phenotype / Phosphorylation / Receptors / Androgen/genetics / Research Support / Non-U.S. Gov't / Vagina/surgery
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26833379
Datenquelle: BASE; Originalkatalog
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Link(s) : http://repub.eur.nl/pub/9738