Authors:
Boehmer, ALM
Nijman, RJM
Lammers, BAS
De Coninck, SJF
Van Hemel, JO
Themmen, APN
Mureau, MAM
De Jong, FH
Brinkmann, AO
Niermeijer, MF
Drop, SLS
Citation: Alm. Boehmer et al., Etiological studies of severe or familial hypospadias, J UROL, 165(4), 2001, pp. 1246-1254
Authors:
Boehmer, ALM
Bruggenwirth, H
Van Assendelft, C
Otten, BJ
Verleun-Mooijman, MCT
Niermeijer, MF
Brunner, HG
Rouwe, CW
Waelkens, JJ
Oostdijk, W
Kleijer, WJ
Van der Kwast, TH
De Vroede, MA
Drop, SLS
Citation: Alm. Boehmer et al., Genotype versus phenotype in families with androgen insensitivity syndrome, J CLIN END, 86(9), 2001, pp. 4151-4160
Authors:
Boehmer, ALM
Brinkmann, AO
Nijman, RM
Verleun-Mooijman, MCT
de Ruiter, P
Niermeijer, MF
Drop, SLS
Citation: Alm. Boehmer et al., Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5 alpha dihydrotestosterone availability, J CLIN END, 86(3), 2001, pp. 1240-1246
Citation: Fme. Slijper et al., Androgen insensitivity syndrome (AIS): Emotional reactions of parents and adult patients to the clinical diagnosis of AIS and its confirmation by androgen receptor gene mutation analysis, HORMONE RES, 53(1), 2000, pp. 9-15
Authors:
Boehmer, ALM
Brinkmann, AO
Sandkuijl, LA
Halley, DJJ
Niermeijer, MF
Andersson, S
de Jong, FH
Kayserili, H
de Vroede, MA
Otten, BJ
Rouwe, CW
Mendonca, BB
Rodrigues, C
Bode, HH
de Ruiter, PE
Delemarre-van de Waal, HA
Drop, SLS
Citation: Alm. Boehmer et al., 17 beta-hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations, J CLIN END, 84(12), 1999, pp. 4713-4721
Authors:
de Zegher, F
Francois, I
Boehmer, ALM
Saggese, G
Muller, J
Hiort, O
Sultan, C
Clayton, P
Brauner, R
Cacciari, E
Ibanez, L
Van Vliet, G
Tiulpakov, A
Saka, N
Ritzen, M
Sippell, WG
Citation: F. De Zegher et al., Androgens and fetal growth, HORMONE RES, 50(4), 1998, pp. 243-244