000			01403 a2200409 4500
005			20250514221114.0
264		0	_c20060331
008			200603s 0 0 eng d
022			_a1468-6244
024	7		_a10.1136/jmg.2004.024505 _2doi
040			_aNLM _beng _cNLM
100	1		_aKim, J-W
245	0	0	_aMMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta. _h[electronic resource]
260			_bJournal of medical genetics _cMar 2005
300			_a271-5 p. _bdigital
500			_aPublication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAmelogenesis Imperfecta _xgenetics
650	0	4	_aBase Sequence
650	0	4	_aChild
650	0	4	_aDNA Mutational Analysis
650	0	4	_aGenes, Recessive
650	0	4	_aHaplotypes
650	0	4	_aHumans
650	0	4	_aMatrix Metalloproteinase 20
650	0	4	_aMatrix Metalloproteinases _xchemistry
650	0	4	_aMolecular Sequence Data
650	0	4	_aPedigree
650	0	4	_aPhenotype
700	1		_aSimmer, J P
700	1		_aHart, T C
700	1		_aHart, P S
700	1		_aRamaswami, M D
700	1		_aBartlett, J D
700	1		_aHu, J C-C
773	0		_tJournal of medical genetics _gvol. 42 _gno. 3 _gp. 271-5
856	4	0	_uhttps://doi.org/10.1136/jmg.2004.024505 _zAvailable from publisher's website
999			_c15417969 _d15417969