17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations

A.L.M. Boehmer; A.O. Brinkmann; L.A. Sandkuijl; D.J.J. Halley; M.F. Nieremeijer; S. Andersson; F.H. de Jong; H. Kayserili; M. de Vroede; B.J. Otten; C.W. Rouwe; B.B. Mendonca; C. Rodrigues; H.H. Bode; P. de Ruiter; H.A. Delemarre-van de Waal; S.L.S. Drop

17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations

A.L.M. Boehmer, A.O. Brinkmann, L.A. Sandkuijl, D.J.J. Halley, M.F. Nieremeijer, S. Andersson, F.H. de Jong, H. Kayserili, M. de Vroede, B.J. Otten, C.W. Rouwe, B.B. Mendonca, C. Rodrigues, H.H. Bode, P. de Ruiter, H.A. Delemarre-van de Waal, S.L.S. Drop

Utrecht University

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	4713-4721
Number of pages	9
Journal	Journal of Clinical Endocrinology and Metabolism
Volume	84
Publication status	Published - 1999

Keywords

Econometric and Statistical Methods: General
Genetics
Geneeskunde(GENK)
Algemeen onderzoek
Overig medisch onderzoek

Cite this

Boehmer, A. L. M., Brinkmann, A. O., Sandkuijl, L. A., Halley, D. J. J., Nieremeijer, M. F., Andersson, S., de Jong, F. H., Kayserili, H., de Vroede, M., Otten, B. J., Rouwe, C. W., Mendonca, B. B., Rodrigues, C., Bode, H. H., de Ruiter, P., Delemarre-van de Waal, H. A., & Drop, S. L. S. (1999). 17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations. Journal of Clinical Endocrinology and Metabolism, 84, 4713-4721.

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title = "17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations",

keywords = "Econometric and Statistical Methods: General, Genetics, Geneeskunde(GENK), Algemeen onderzoek, Overig medisch onderzoek",

author = "A.L.M. Boehmer and A.O. Brinkmann and L.A. Sandkuijl and D.J.J. Halley and M.F. Nieremeijer and S. Andersson and {de Jong}, F.H. and H. Kayserili and {de Vroede}, M. and B.J. Otten and C.W. Rouwe and B.B. Mendonca and C. Rodrigues and H.H. Bode and {de Ruiter}, P. and {Delemarre-van de Waal}, H.A. and S.L.S. Drop",

year = "1999",

language = "Undefined/Unknown",

volume = "84",

pages = "4713--4721",

journal = "Journal of Clinical Endocrinology and Metabolism",

issn = "0021-972X",

publisher = "The Endocrine Society",

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Boehmer, ALM, Brinkmann, AO, Sandkuijl, LA, Halley, DJJ, Nieremeijer, MF, Andersson, S, de Jong, FH, Kayserili, H, de Vroede, M, Otten, BJ, Rouwe, CW, Mendonca, BB, Rodrigues, C, Bode, HH, de Ruiter, P, Delemarre-van de Waal, HA & Drop, SLS 1999, '17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations', Journal of Clinical Endocrinology and Metabolism, vol. 84, pp. 4713-4721.

17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations. / Boehmer, A.L.M.; Brinkmann, A.O.; Sandkuijl, L.A. et al.
In: Journal of Clinical Endocrinology and Metabolism, Vol. 84, 1999, p. 4713-4721.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - 17-Hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations

AU - Boehmer, A.L.M.

AU - Brinkmann, A.O.

AU - Sandkuijl, L.A.

AU - Halley, D.J.J.

AU - Nieremeijer, M.F.

AU - Andersson, S.

AU - de Jong, F.H.

AU - Kayserili, H.

AU - de Vroede, M.

AU - Otten, B.J.

AU - Rouwe, C.W.

AU - Mendonca, B.B.

AU - Rodrigues, C.

AU - Bode, H.H.

AU - de Ruiter, P.

AU - Delemarre-van de Waal, H.A.

AU - Drop, S.L.S.

PY - 1999

Y1 - 1999

KW - Econometric and Statistical Methods: General

KW - Genetics

KW - Geneeskunde(GENK)

KW - Algemeen onderzoek

KW - Overig medisch onderzoek

M3 - Article

SN - 0021-972X

VL - 84

SP - 4713

EP - 4721

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

ER -