000			01168 a2200373 4500
005			20250511131624.0
264		0	_c19800324
008			198003s 0 0 eng d
022			_a0361-7742
040			_aNLM _beng _cNLM
100	1		_aSvejgaard, A
245	0	0	_aHLA markers and disease. _h[electronic resource]
260			_bProgress in clinical and biological research _c1979
300			_a523-43 p. _bdigital
500			_aPublication Type: Journal Article; Review
650	0	4	_aAdrenocortical Hyperfunction _xgenetics
650	0	4	_aChild
650	0	4	_aChromosomes, Human, 6-12 and X
650	0	4	_aComplement C2 _xdeficiency
650	0	4	_aDiabetes Mellitus _xgenetics
650	0	4	_aFemale
650	0	4	_aGene Frequency
650	0	4	_aGenetic Diseases, Inborn _ximmunology
650	0	4	_aGenetic Linkage
650	0	4	_aHLA Antigens _xgenetics
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aPsoriasis _xgenetics
650	0	4	_aRacial Groups
650	0	4	_aRecombination, Genetic
650	0	4	_aSpondylitis, Ankylosing _xgenetics
700	1		_aRyder, L P
773	0		_tProgress in clinical and biological research _gvol. 32 _gp. 523-43
999			_c413384 _d413384