000 01697 a2200481 4500
005 20250513195936.0
264 0 _c19991222
008 199912s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/(sici)1096-8628(19991203)87:4<324::aid-ajmg8>3.0.co;2-u
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLabrune, P
245 0 0 _aJeune syndrome and liver disease: report of three cases treated with ursodeoxycholic acid.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cDec 1999
300 _a324-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAlanine Transaminase
_xblood
650 0 4 _aAspartate Aminotransferases
_xblood
650 0 4 _aAsphyxia Neonatorum
_xcomplications
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCholagogues and Choleretics
_xtherapeutic use
650 0 4 _aFemale
650 0 4 _aFollow-Up Studies
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aLiver Diseases
_xcomplications
650 0 4 _aMale
650 0 4 _aOsteochondrodysplasias
_xcomplications
650 0 4 _aTreatment Outcome
650 0 4 _aUrsodeoxycholic Acid
_xtherapeutic use
650 0 4 _agamma-Glutamyltransferase
_xblood
700 1 _aFabre, M
700 1 _aTrioche, P
700 1 _aEstournet-Mathiaud, B
700 1 _aGrangeponte, M C
700 1 _aRambaud, C
700 1 _aMaurage, C
700 1 _aBernard, O
773 0 _tAmerican journal of medical genetics
_gvol. 87
_gno. 4
_gp. 324-8
856 4 0 _uhttps://doi.org/10.1002/(sici)1096-8628(19991203)87:4<324::aid-ajmg8>3.0.co;2-u
_zAvailable from publisher's website
999 _c10544998
_d10544998