000 01329 a2200421 4500
005 20250515195430.0
264 0 _c20100224
008 201002s 0 0 eng d
022 _a1526-3347
024 7 _a10.1542/pir.30-12-479
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFerrarini, Alessandra
245 0 0 _aIndex of suspicion.
_h[electronic resource]
260 _bPediatrics in review
_cDec 2009
300 _a479-85 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAcidosis, Renal Tubular
_xdiagnosis
650 0 4 _aChild
650 0 4 _aFollow-Up Studies
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aOculocerebrorenal Syndrome
_xdiagnosis
650 0 4 _aRare Diseases
650 0 4 _aRisk Assessment
650 0 4 _aSampling Studies
650 0 4 _aTelangiectasia, Hereditary Hemorrhagic
_xdiagnosis
700 1 _aRamelli, Gian Paolo
700 1 _aBianchetti, Mario G
700 1 _aHedman, Jamie
700 1 _aSharathkumar, Anjali
700 1 _aShapiro, Amy
700 1 _aBourland, Christina
773 0 _tPediatrics in review
_gvol. 30
_gno. 12
_gp. 479-85
856 4 0 _uhttps://doi.org/10.1542/pir.30-12-479
_zAvailable from publisher's website
999 _c19335543
_d19335543