Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.

B.I. Hendriks-Stegeman; K.D. Augustijn; B.F.M. Bakker; P. Holthuizen; P.C. van der Vliet; M. Jansen

Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.

Translated title of the contribution: Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.

B.I. Hendriks-Stegeman, K.D. Augustijn, B.F.M. Bakker, P. Holthuizen, P.C. van der Vliet, M. Jansen

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

Translated title of the contribution	Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.
Original language	Undefined/Unknown
Pages (from-to)	1545-1550
Number of pages	6
Journal	Journal of Clinical Endocrinology and Metabolism
Volume	86
Issue number	4
Publication status	Published - 2001

Keywords

Econometric and Statistical Methods: General
Geneeskunde (GENK)
Genetics
Geneeskunde(GENK)
Algemeen onderzoek
Internal medicine

Cite this

@article{96207cea363748919d8891e360ceb6db,

title = "Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.",

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

author = "B.I. Hendriks-Stegeman and K.D. Augustijn and B.F.M. Bakker and P. Holthuizen and {van der Vliet}, P.C. and M. Jansen",

year = "2001",

language = "Undefined/Unknown",

volume = "86",

pages = "1545--1550",

journal = "Journal of Clinical Endocrinology and Metabolism",

issn = "0021-972X",

publisher = "Endocrine Society",

number = "4",

}

Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene. / Hendriks-Stegeman, B.I.; Augustijn, K.D.; Bakker, B.F.M. et al.
In: Journal of Clinical Endocrinology and Metabolism, Vol. 86, No. 4, 2001, p. 1545-1550.

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

TY - JOUR

T1 - Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POU1F1 gene.

AU - Hendriks-Stegeman, B.I.

AU - Augustijn, K.D.

AU - Bakker, B.F.M.

AU - Holthuizen, P.

AU - van der Vliet, P.C.

AU - Jansen, M.

PY - 2001

Y1 - 2001

KW - Econometric and Statistical Methods: General

KW - Geneeskunde (GENK)

KW - Genetics

KW - Geneeskunde(GENK)

KW - Algemeen onderzoek

KW - Internal medicine

M3 - Article

SN - 0021-972X

VL - 86

SP - 1545

EP - 1550

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

IS - 4

ER -