000 01162 a2200325 4500
005 20250513223819.0
264 0 _c20010215
008 200102s 0 0 eng d
022 _a0009-9163
024 7 _a10.1034/j.1399-0004.2000.580301.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSutherland, G R
245 0 0 _aThe clinical significance of fragile sites on human chromosomes.
_h[electronic resource]
260 _bClinical genetics
_cSep 2000
300 _a157-61 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aChromosome Aberrations
_xclassification
650 0 4 _aChromosome Disorders
650 0 4 _aChromosome Fragile Sites
650 0 4 _aChromosome Fragility
_xgenetics
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aPrenatal Diagnosis
650 0 4 _aX Chromosome
_xgenetics
700 1 _aBaker, E
773 0 _tClinical genetics
_gvol. 58
_gno. 3
_gp. 157-61
856 4 0 _uhttps://doi.org/10.1034/j.1399-0004.2000.580301.x
_zAvailable from publisher's website
999 _c11017788
_d11017788