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

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10.1111/cen.13760

Hovinga_et_al-2018-Clinical_EndocrinologyFinal published version, 430 KBLicence: Taverne

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@article{53b3c50ffe6e4d85b57ac32a546865ea,

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 Publishing Ltd",

number = "3",

}

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 - https://www.scopus.com/pages/publications/85050450910

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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