A.L. Boehmer
Department of Pediatrics
Sophia Children's Hospital
Rotterdam
Netherlands
Name/email consistency: high
- 17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations. Boehmer, A.L., Brinkmann, A.O., Sandkuijl, L.A., Halley, D.J., Niermeijer, M.F., Andersson, S., de Jong, F.H., Kayserili, H., de Vroede, M.A., Otten, B.J., Rouwé, C.W., Mendonça, B.B., Rodrigues, C., Bode, H.H., de Ruiter, P.E., Delemarre-van de Waal, H.A., Drop, S.L. J. Clin. Endocrinol. Metab. (1999)