000 01307 a2200397 4500
005 20250513204745.0
264 0 _c20000428
008 200004s 0 0 eng d
022 _a0009-9163
024 7 _a10.1034/j.1399-0004.2000.570116.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCarpenter, N J
245 0 0 _a'Novel' immunodeficiency syndrome may be a previously described entity.
_h[electronic resource]
260 _bClinical genetics
_cJan 2000
300 _a90-2 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Comment
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aCraniosynostoses
_xgenetics
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aGenetic Linkage
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aImmunoglobulin G
_xblood
650 0 4 _aImmunologic Deficiency Syndromes
_xgenetics
650 0 4 _aInfections
_xgenetics
650 0 4 _aMale
650 0 4 _aMicrocephaly
_xgenetics
650 0 4 _aPolymorphism, Genetic
650 0 4 _aX Chromosome
700 1 _aBerkel, I
700 1 _aSay, B
773 0 _tClinical genetics
_gvol. 57
_gno. 1
_gp. 90-2
856 4 0 _uhttps://doi.org/10.1034/j.1399-0004.2000.570116.x
_zAvailable from publisher's website
999 _c10686785
_d10686785