000 01531 a2200469 4500
005 20250513113139.0
264 0 _c19970408
008 199704s 0 0 eng d
022 _a0022-3476
024 7 _a10.1016/s0022-3476(97)70199-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBuckley, R H
245 0 0 _aHuman severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.
_h[electronic resource]
260 _bThe Journal of pediatrics
_cMar 1997
300 _a378-87 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdenosine Deaminase
_xdeficiency
650 0 4 _aFemale
650 0 4 _aGenes, Recessive
650 0 4 _aGenetic Linkage
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aImmunoglobulins
_xblood
650 0 4 _aImmunophenotyping
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aJanus Kinase 3
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aProtein-Tyrosine Kinases
_xdeficiency
650 0 4 _aSevere Combined Immunodeficiency
_xgenetics
650 0 4 _aX Chromosome
700 1 _aSchiff, R I
700 1 _aSchiff, S E
700 1 _aMarkert, M L
700 1 _aWilliams, L W
700 1 _aHarville, T O
700 1 _aRoberts, J L
700 1 _aPuck, J M
773 0 _tThe Journal of pediatrics
_gvol. 130
_gno. 3
_gp. 378-87
856 4 0 _uhttps://doi.org/10.1016/s0022-3476(97)70199-9
_zAvailable from publisher's website
999 _c9051191
_d9051191