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 https://doi.org/10.1111/cen.13760
Publication status	Published - 1 Sept 2018

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Kremer Hovinga, I. C. L., Giltay, J. C., van der Crabben, S. N., Steyls, A., van der Kamp, H. J., & Paulussen, A. D. C. (2018). Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications. Clinical Endocrinology, 89(3), 378-380. https://doi.org/10.1111/cen.13760, https://doi.org/10.1111/cen.13760

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

author = "{Kremer Hovinga}, {Idske C.L.} 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",

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Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications. / Kremer Hovinga, Idske C.L.; 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

T2 - clinical implications

AU - Kremer Hovinga, Idske C.L.

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

UR - http://www.scopus.com/inward/record.url?scp=85050450910&partnerID=8YFLogxK

U2 - 10.1111/cen.13760

DO - 10.1111/cen.13760

M3 - Comment/Letter to the editor

C2 - 29876959

AN - SCOPUS:85050450910

SN - 0300-0664

VL - 89

SP - 378

EP - 380

JO - Clinical Endocrinology

JF - Clinical Endocrinology

IS - 3

ER -

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

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