TY  - GEN
AU  - Alatzoglou,Kyriaki S
AU  - Turton,James P
AU  - Kelberman,Daniel
AU  - Clayton,Peter E
AU  - Mehta,Ameeta
AU  - Buchanan,Charles
AU  - Aylwin,Simon
AU  - Crowne,Elisabeth C
AU  - Christesen,Henrik T
AU  - Hertel,Niels T
AU  - Trainer,Peter J
AU  - Savage,Martin O
AU  - Raza,Jamal
AU  - Banerjee,Kausik
AU  - Sinha,Sunil K
AU  - Ten,Svetlana
AU  - Mushtaq,Talat
AU  - Brauner,Raja
AU  - Cheetham,Timothy D
AU  - Hindmarsh,Peter C
AU  - Mullis,Primus E
AU  - Dattani,Mehul T
TI  - Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency
SN  - 1945-7197
PY  - 2009///0923
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Genetic Testing
KW  - Homeodomain Proteins
KW  - genetics
KW  - Human Growth Hormone
KW  - deficiency
KW  - Humans
KW  - Infant
KW  - Locus Control Region
KW  - Mutation
KW  - Pedigree
KW  - Receptors, Neuropeptide
KW  - Receptors, Pituitary Hormone-Regulating Hormone
KW  - SOXB1 Transcription Factors
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1210/jc.2008-2783
ER  -