000			01705 a2200541 4500
005			20250514195320.0
264		0	_c20050310
008			200503s 0 0 eng d
022			_a1098-1004
024	7		_a10.1002/humu.20079 _2doi
040			_aNLM _beng _cNLM
100	1		_aBeysen, Diane
245	0	0	_aThe human FOXL2 mutation database. _h[electronic resource]
260			_bHuman mutation _cSep 2004
300			_a189-93 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAlleles
650	0	4	_aBlepharophimosis _xgenetics
650	0	4	_aChromosomes, Human, Pair 3 _xgenetics
650	0	4	_aDNA-Binding Proteins _xchemistry
650	0	4	_aDatabases, Genetic
650	0	4	_aFemale
650	0	4	_aForkhead Box Protein L2
650	0	4	_aForkhead Transcription Factors
650	0	4	_aGene Expression Regulation, Developmental _xgenetics
650	0	4	_aGenes
650	0	4	_aGenes, Dominant
650	0	4	_aGenetic Heterogeneity
650	0	4	_aGenetic Variation
650	0	4	_aHumans
650	0	4	_aInternet
650	0	4	_aMale
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation
650	0	4	_aPhenotype
650	0	4	_aPolymorphism, Genetic
650	0	4	_aPrimary Ovarian Insufficiency _xgenetics
650	0	4	_aSoftware
650	0	4	_aSyndrome
650	0	4	_aTranscription Factors _xchemistry
650	0	4	_aUser-Computer Interface
700	1		_aVandesompele, Jo
700	1		_aMessiaen, Ludwine
700	1		_aDe Paepe, Anne
700	1		_aDe Baere, Elfride
773	0		_tHuman mutation _gvol. 24 _gno. 3 _gp. 189-93
856	4	0	_uhttps://doi.org/10.1002/humu.20079 _zAvailable from publisher's website
999			_c15000498 _d15000498