Genotype Versus phenotype in families with androgen insensitivity syndrome

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 9, 2001, Pages 4151-4160

  Boehmer, Annemie L M ^a,g,h   Brüggenwirth, Hennie ^g   Van Assendelft, Cissy ^a   Otten, Barto J ^b   Verleun Mooijman, Marja C T ^g   Niermeijer, Martinus F ^h   Brunner, Han G ^b   Rouwé, Catrienus W ^c   Waelkens, J J ^d   Oostdijk, Wilma ^e   Kleijer, Wim J ^h   Van Der Kwast, Theo H ^g   De Vroede, Monique A ^f   Drop, Stenvert L S ^a  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^d CATHARINA HOSPITAL   (Netherlands)

^e LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^f UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^g ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^h ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; CLINICAL ARTICLE; EMBRYO DEVELOPMENT; GENE DELETION; GENE MUTATION; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENOTYPE; HUMAN; MALE; MICROPENIS; MOSAICISM; MULTIGENE FAMILY; NETHERLANDS; PHENOTYPE; PRIORITY JOURNAL; SKIN FIBROBLAST; VIRILIZATION;

WOLFFIA;

EID: 17944370006     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.9.7825     Document Type: Article

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