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

L.C.G. Graaff; J. Argente; D.C.M. Veenma; M.L. Drent; A.G. Uitterlinden; A.C.S. 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

L.C.G. Graaff, J. Argente, D.C.M. Veenma, M.L. Drent, A.G. Uitterlinden, A.C.S. Hokken-Koelega

Internal medicine

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

Original language	Undefined/Unknown
Pages (from-to)	363-371
Journal	Hormone Research in Paediatrics
Volume	73
Issue number	5
DOIs	https://doi.org/10.1159/000308169
Publication status	Published - 2010

Access to Document

10.1159/000308169

Cite this

Graaff, L. C. G., Argente, J., Veenma, D. C. M., Drent, M. L., Uitterlinden, A. G., & Hokken-Koelega, A. C. S. (2010). 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. Hormone Research in Paediatrics, 73(5), 363-371. https://doi.org/10.1159/000308169

Graaff, L.C.G. ; Argente, J. ; Veenma, D.C.M. ; Drent, M.L. ; Uitterlinden, A.G. ; Hokken-Koelega, A.C.S. / 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. In: Hormone Research in Paediatrics. 2010 ; Vol. 73, No. 5. pp. 363-371.

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Graaff, LCG, Argente, J, Veenma, DCM, Drent, ML, Uitterlinden, AG & Hokken-Koelega, ACS 2010, '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', Hormone Research in Paediatrics, vol. 73, no. 5, pp. 363-371. https://doi.org/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. / Graaff, L.C.G.; Argente, J.; Veenma, D.C.M.; Drent, M.L.; Uitterlinden, A.G.; Hokken-Koelega, A.C.S.

In: Hormone Research in Paediatrics, Vol. 73, No. 5, 2010, p. 363-371.

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

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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 - Graaff, L.C.G.

AU - Argente, J.

AU - Veenma, D.C.M.

AU - Drent, M.L.

AU - Uitterlinden, A.G.

AU - Hokken-Koelega, A.C.S.

PY - 2010

Y1 - 2010

U2 - 10.1159/000308169

DO - 10.1159/000308169

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VL - 73

SP - 363

EP - 371

JO - Hormone Research in Paediatrics

JF - Hormone Research in Paediatrics

SN - 1663-2818

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