Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications

Idske C. L. Kremer Hovinga; Jacques C. Giltay; Saskia N. van der Crabben; Anja Steyls; Hetty J. van der Kamp; Aimee D. C. Paulussen

doi:10.1111/cen.13760

Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications

Idske C. L. Kremer Hovinga^*
, Jacques C. Giltay
, Saskia N. van der Crabben
, Anja Steyls
, Hetty J. van der Kamp
, Aimee D. C. Paulussen

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

Original language	English
Pages (from-to)	378-380
Number of pages	3
Journal	Clinical Endocrinology
Volume	89
Issue number	3
DOIs	https://doi.org/10.1111/cen.13760
Publication status	Published - 1 Sept 2018

Keywords

HYPOPITUITARISM

Access to Document

10.1111/cen.13760

Cite this

@article{4272c8e3d2cb4c26bfc880f61fb8e145,

title = "Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications",

keywords = "HYPOPITUITARISM",

author = "Hovinga, \{Idske C. L. Kremer\} and Giltay, \{Jacques C.\} and \{van der Crabben\}, \{Saskia N.\} and Anja Steyls and \{van der Kamp\}, \{Hetty J.\} and Paulussen, \{Aimee D. C.\}",

year = "2018",

month = sep,

day = "1",

doi = "10.1111/cen.13760",

language = "English",

volume = "89",

pages = "378--380",

journal = "Clinical Endocrinology",

issn = "0300-0664",

publisher = "Wiley-Blackwell",

number = "3",

}

Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications. / Hovinga, Idske C. L. Kremer; Giltay, Jacques C.; van der Crabben, Saskia N. et al.
In: Clinical Endocrinology, Vol. 89, No. 3, 01.09.2018, p. 378-380.

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

TY - JOUR

T1 - Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications

AU - Hovinga, Idske C. L. Kremer

AU - Giltay, Jacques C.

AU - van der Crabben, Saskia N.

AU - Steyls, Anja

AU - van der Kamp, Hetty J.

AU - Paulussen, Aimee D. C.

PY - 2018/9/1

Y1 - 2018/9/1

KW - HYPOPITUITARISM

U2 - 10.1111/cen.13760

DO - 10.1111/cen.13760

M3 - Comment/Letter to the editor

SN - 0300-0664

VL - 89

SP - 378

EP - 380

JO - Clinical Endocrinology

JF - Clinical Endocrinology

IS - 3

ER -