Extreme phenotypic variability of a novel GLI2 mutation in a large family with panhypopituitarism and polydactyly: clinical implications
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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.; Steyls, Anja; van der Kamp, Hetty J.; Paulussen, Aimee D.C.
(2018) Clinical Endocrinology, volume 89, issue 3, pp. 378 - 380
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Keywords: Endocrinology, Diabetes and Metabolism
DOI:
https://doi.org/10.1111/cen.13760
ISSN: 0300-0664
Publisher: Wiley-Blackwell
(Peer reviewed)