PROP1, HESX1, POU1F1. LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency

Laura de Graaff; J Argente; Danielle Veenma; M Drent; André Uitterlinden; Anita Hokken - Koelega

doi:10.1159/000308169

PROP1, HESX1, POU1F1. LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency

Laura de Graaff, J Argente, Danielle Veenma, M Drent, André Uitterlinden, Anita Hokken - Koelega

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

32 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	363-371
Number of pages	9
Journal	Hormone Research
Volume	73
DOIs	https://doi.org/10.1159/000308169
Publication status	Published - 2010

Research programs

EMC MM-01-39-02
EMC MM-01-54-01

Access to Document

10.1159/000308169

http://hdl.handle.net/1765/20188

Cite this

@article{6d08a6ca0e11448098c9703ed1be9cf5,

title = "PROP1, HESX1, POU1F1. LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency",

author = "{de Graaff}, Laura and J Argente and Danielle Veenma and M Drent and Andr{\'e} Uitterlinden and {Hokken - Koelega}, Anita",

year = "2010",

doi = "10.1159/000308169",

language = "Undefined/Unknown",

volume = "73",

pages = "363--371",

journal = "Hormone Research",

issn = "0301-0163",

publisher = "Karger",

}

PROP1, HESX1, POU1F1. LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency. / de Graaff, Laura; Argente, J; Veenma, Danielle et al.
In: Hormone Research, Vol. 73, 2010, p. 363-371.

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

TY - JOUR

T1 - PROP1, HESX1, POU1F1. LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency

AU - de Graaff, Laura

AU - Argente, J

AU - Veenma, Danielle

AU - Drent, M

AU - Uitterlinden, André

AU - Hokken - Koelega, Anita

PY - 2010

Y1 - 2010

U2 - 10.1159/000308169

DO - 10.1159/000308169

M3 - Article

C2 - 20389107

SN - 0301-0163

VL - 73

SP - 363

EP - 371

JO - Hormone Research

JF - Hormone Research

ER -