000 01152 a2200313 4500
005 20250517235649.0
264 0 _c20190523
008 201905s 0 0 eng d
022 _a1551-3823
024 7 _a10.1080/15513815.2018.1485797
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTan, April W
245 0 0 _aTokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
_h[electronic resource]
260 _bFetal and pediatric pathology
_cAug 2018
300 _a296-300 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAnkyrins
_xdeficiency
650 0 4 _aCodon, Nonsense
650 0 4 _aFemale
650 0 4 _aHispanic or Latino
_xgenetics
650 0 4 _aHumans
650 0 4 _aHyperbilirubinemia, Neonatal
_xgenetics
650 0 4 _aInfant, Newborn
650 0 4 _aSpherocytosis, Hereditary
_xcomplications
700 1 _aLeung, Pablo
700 1 _aPatil, Uday P
773 0 _tFetal and pediatric pathology
_gvol. 37
_gno. 4
_gp. 296-300
856 4 0 _uhttps://doi.org/10.1080/15513815.2018.1485797
_zAvailable from publisher's website
999 _c28828246
_d28828246