000 01454 a2200469 4500
005 20250514221851.0
264 0 _c20051215
008 200512s 0 0 spa d
022 _a0034-9887
024 7 _a10.4067/s0034-98872005000100005
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCortés M, Fanny
245 0 0 _a[Clinical, genetic and molecular features in 45 patients with Prader-Willi syndrome].
_h[electronic resource]
260 _bRevista medica de Chile
_cJan 2005
300 _a33-41 p.
_bdigital
500 _aPublication Type: English Abstract; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChile
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMethylation
650 0 4 _aPhenotype
650 0 4 _aPrader-Willi Syndrome
_xdiagnosis
650 0 4 _aRetrospective Studies
700 1 _aAlliende R, M Angélica
700 1 _aBarrios R, Andrés
700 1 _aCurotto L, Bianca
700 1 _aSanta María V, Lorena
700 1 _aBarraza O, Ximena
700 1 _aTroncoso A, Ledia
700 1 _aMellado S, Cecilia
700 1 _aPardo V, Rosa
773 0 _tRevista medica de Chile
_gvol. 133
_gno. 1
_gp. 33-41
856 4 0 _uhttps://doi.org/10.4067/s0034-98872005000100005
_zAvailable from publisher's website
999 _c15440799
_d15440799