000			01849 a2200589 4500
005			20250513130301.0
264		0	_c19971119
008			199711s 0 0 eng d
022			_a0340-6717
024	7		_a10.1007/s004390050542 _2doi
040			_aNLM _beng _cNLM
100	1		_aMilà, M
245	0	0	_aScreening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation. _h[electronic resource]
260			_bHuman genetics _cOct 1997
300			_a503-7 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosome Fragile Sites
650	0	4	_aChromosome Fragility
650	0	4	_aDNA Methylation
650	0	4	_aFemale
650	0	4	_aFragile X Mental Retardation Protein
650	0	4	_aFragile X Syndrome _xgenetics
650	0	4	_aGenetic Testing
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMosaicism
650	0	4	_aMutation _xgenetics
650	0	4	_aNerve Tissue Proteins _xgenetics
650	0	4	_aNuclear Proteins
650	0	4	_aPhenotype
650	0	4	_aProteins _xgenetics
650	0	4	_aPsychotic Disorders _xgenetics
650	0	4	_aRNA-Binding Proteins
650	0	4	_aSchools
650	0	4	_aSpain
650	0	4	_aTrans-Activators
650	0	4	_aTrinucleotide Repeats _xgenetics
650	0	4	_aX Chromosome _xgenetics
700	1		_aSànchez, A
700	1		_aBadenas, C
700	1		_aBrun, C
700	1		_aJiménez, D
700	1		_aVilla, M P
700	1		_aCastellví-Bel, S
700	1		_aEstivill, X
773	0		_tHuman genetics _gvol. 100 _gno. 5-6 _gp. 503-7
856	4	0	_uhttps://doi.org/10.1007/s004390050542 _zAvailable from publisher's website
999			_c9313159 _d9313159