000 01495 a2200457 4500
005 20250516183425.0
264 0 _c20140717
008 201407s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/1750-1172-8-187
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFernández, Raquel M
245 0 0 _aPathways systematically associated to Hirschsprung's disease.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cDec 2013
300 _a187 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenotype
650 0 4 _aHirschsprung Disease
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
700 1 _aBleda, Marta
700 1 _aLuzón-Toro, Berta
700 1 _aGarcía-Alonso, Luz
700 1 _aArnold, Stacey
700 1 _aSribudiani, Yunia
700 1 _aBesmond, Claude
700 1 _aLantieri, Francesca
700 1 _aDoan, Betty
700 1 _aCeccherini, Isabella
700 1 _aLyonnet, Stanislas
700 1 _aHofstra, Robert Mw
700 1 _aChakravarti, Aravinda
700 1 _aAntiñolo, Guillermo
700 1 _aDopazo, Joaquín
700 1 _aBorrego, Salud
773 0 _tOrphanet journal of rare diseases
_gvol. 8
_gp. 187
856 4 0 _uhttps://doi.org/10.1186/1750-1172-8-187
_zAvailable from publisher's website
999 _c23321143
_d23321143