000			01804 a2200493 4500
005			20250512031647.0
264		0	_c19861008
008			198610s 0 0 eng d
022			_a0021-9738
024	7		_a10.1172/JCI112623 _2doi
040			_aNLM _beng _cNLM
100	1		_aSchneider, P M
245	0	0	_aPolymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants. _h[electronic resource]
260			_bThe Journal of clinical investigation _cSep 1986
300			_a650-7 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAdrenal Hyperplasia, Congenital _xgenetics
650	0	4	_aAlleles
650	0	4	_aCeliac Disease _xgenetics
650	0	4	_aChromosome Aberrations
650	0	4	_aChromosome Deletion
650	0	4	_aComplement C4 _xgenetics
650	0	4	_aDNA _xgenetics
650	0	4	_aDNA Restriction Enzymes
650	0	4	_aDeoxyribonucleases, Type II Site-Specific
650	0	4	_aGenes
650	0	4	_aHaploidy
650	0	4	_aHumans
650	0	4	_aMajor Histocompatibility Complex
650	0	4	_aMultiple Sclerosis _xgenetics
650	0	4	_aNucleic Acid Hybridization
650	0	4	_aPhenotype
650	0	4	_aPolymorphism, Genetic
650	0	4	_aSteroid 21-Hydroxylase _xgenetics
650	0	4	_aSteroid Hydroxylases _xgenetics
700	1		_aCarroll, M C
700	1		_aAlper, C A
700	1		_aRittner, C
700	1		_aWhitehead, A S
700	1		_aYunis, E J
700	1		_aColten, H R
773	0		_tThe Journal of clinical investigation _gvol. 78 _gno. 3 _gp. 650-7
856	4	0	_uhttps://doi.org/10.1172/JCI112623 _zAvailable from publisher's website
999			_c3023857 _d3023857