000			01378 a2200445 4500
005			20250513001925.0
264		0	_c19821029
008			198210s 0 0 eng d
022			_a0340-6717
024	7		_a10.1007/BF00569212 _2doi
040			_aNLM _beng _cNLM
100	1		_aSchmidt, A
245	0	0	_aFragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds. _h[electronic resource]
260			_bHuman genetics _c1982
300			_a322-7 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	_aAge Factors
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromosome Fragile Sites
650	0	4	_aChromosome Fragility
650	0	4	_aFemale
650	0	4	_aGenetic Linkage
650	0	4	_aGenetic Markers
650	0	4	_aHeterozygote
650	0	4	_aHumans
650	0	4	_aInfant
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aLymphocytes _xcytology
650	0	4	_aMale
650	0	4	_aMetaphase
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aSex Chromosomes
650	0	4	_aX Chromosome
773	0		_tHuman genetics _gvol. 60 _gno. 4 _gp. 322-7
856	4	0	_uhttps://doi.org/10.1007/BF00569212 _zAvailable from publisher's website
999			_c6954937 _d6954937