000 01657 a2200529 4500
005 20250515083059.0
264 0 _c20080102
008 200801s 0 0 eng d
022 _a0021-972X
024 7 _a10.1210/jc.2007-0684
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHess, Ora
245 0 0 _aVariable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.
_h[electronic resource]
260 _bThe Journal of clinical endocrinology and metabolism
_cNov 2007
300 _a4387-93 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aArabs
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHuman Growth Hormone
_xblood
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInsulin-Like Growth Factor I
_xmetabolism
650 0 4 _aJews
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aTwins
700 1 _aHujeirat, Yasir
700 1 _aWajnrajch, Michael P
700 1 _aAllon-Shalev, Stavit
700 1 _aZadik, Zvi
700 1 _aLavi, Idit
700 1 _aTenenbaum-Rakover, Yardena
773 0 _tThe Journal of clinical endocrinology and metabolism
_gvol. 92
_gno. 11
_gp. 4387-93
856 4 0 _uhttps://doi.org/10.1210/jc.2007-0684
_zAvailable from publisher's website
999 _c17314264
_d17314264