000 01618 a2200517 4500
005 20250515153709.0
264 0 _c20090803
008 200908s 0 0 eng d
022 _a1365-2265
024 7 _a10.1111/j.1365-2265.2008.03326.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKelberman, D
245 0 0 _aMolecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).
_h[electronic resource]
260 _bClinical endocrinology
_cJan 2009
300 _a96-103 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAnimals
650 0 4 _aCHO Cells
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCohort Studies
650 0 4 _aCricetinae
650 0 4 _aCricetulus
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHomeodomain Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aHypopituitarism
_xgenetics
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aPituitary Hormones
_xdeficiency
700 1 _aTurton, J P G
700 1 _aWoods, K S
700 1 _aMehta, A
700 1 _aAl-Khawari, M
700 1 _aGreening, J
700 1 _aSwift, P G F
700 1 _aOtonkoski, T
700 1 _aRhodes, S J
700 1 _aDattani, M T
773 0 _tClinical endocrinology
_gvol. 70
_gno. 1
_gp. 96-103
856 4 0 _uhttps://doi.org/10.1111/j.1365-2265.2008.03326.x
_zAvailable from publisher's website
999 _c18577536
_d18577536