Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions News feed Embed this list Save this search Mark all Export Your filters: cql: author exact 801001092925 cql: author exact 001980177905 Mark journalArticle A1 open access Extensive clinical, hormonal and genetic screening in a large consecutive series of 46, XY neonates and infants with atypical sexual development Dorien Baetens (UGent) , Wilhelm Mladenov, BARBARA DELLE CHIAIE (UGent) , Björn Menten (UGent) , An Desloovere (UGent) , Violeta Iotova, Bert Callewaert (UGent) , Erik Van Laecke (UGent) , Piet Hoebeke (UGent) , Elfride De Baere (UGent) , et al. (2014) ORPHANET JOURNAL OF RARE DISEASES. 9. Mark misc A novel mutation c.118delA in exon 1 of the androgen receptor gene resulting in complete androgen insensitivity syndrome within a large family Karel Decaestecker (UGent) , Pascal Philibert, Elfride De Baere (UGent) , Piet Hoebeke (UGent) , Jean Kaufman (UGent) , Charles Sultan and Guy T'Sjoen (UGent) (2008) FERTILITY AND STERILITY. 89(5).