R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata.

Hormones (Athens, Greece)

Volumn 5, Issue 3, 2006, Pages 200-204

  Goulis, Dimitrios G ^a   Iliadou, Paschalia K ^a   Papanicolaou, Athanasios ^a   Georgiou, Ioannis ^a   Chatzikyriakidou, Anthi ^a   Gerou, Spiridon ^a   Bondis, Ioannis N ^a   Papadimas, Ioannis ^a  

^a ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; ANDROSTANOLONE; FOLLITROPIN; GLYCOPROTEIN; MULLERIAN INHIBITING HORMONE; MULLERIAN-INHIBITING HORMONE; TESTIS PEPTIDE HORMONE;

ADOLESCENT; ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; BLOOD; CASE REPORT; FEMALE; GENETICS; HAMARTOMA; HUMAN; KARYOTYPING; LEYDIG CELL; MALE; PHENOTYPE; POINT MUTATION; SERTOLI CELL; TESTIS DISEASE; ULTRASTRUCTURE;

ADOLESCENT; ANDROGEN-INSENSITIVITY SYNDROME; DIHYDROTESTOSTERONE; FEMALE; FOLLICLE STIMULATING HORMONE; GLYCOPROTEINS; HAMARTOMA; HUMANS; KARYOTYPING; LEYDIG CELLS; MALE; PHENOTYPE; POINT MUTATION; RECEPTORS, ANDROGEN; SERTOLI CELLS; TESTICULAR DISEASES; TESTICULAR HORMONES;

EID: 33750612246     PISSN: 11093099     EISSN: None     Source Type: Journal    
DOI: 10.14310/horm.2002.11185     Document Type: Article

References (0)