Back to Search Start Over

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

Authors :
Kremer Hovinga ICL
Giltay JC
van der Crabben SN
Steyls A
van der Kamp HJ
Paulussen ADC
Source :
Clinical endocrinology [Clin Endocrinol (Oxf)] 2018 Sep; Vol. 89 (3), pp. 378-380. Date of Electronic Publication: 2018 Jul 03.
Publication Year :
2018

Details

Language :
English
ISSN :
1365-2265
Volume :
89
Issue :
3
Database :
MEDLINE
Journal :
Clinical endocrinology
Publication Type :
Editorial & Opinion
Accession number :
29876959
Full Text :
https://doi.org/10.1111/cen.13760