000 01597 a2200493 4500
005 20250513052400.0
264 0 _c19941116
008 199411s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320510405
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChiurazzi, P
245 0 0 _aNo apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cJul 1994
300 _a309-14 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFragile X Mental Retardation Protein
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGenes
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xetiology
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aNerve Tissue Proteins
_xbiosynthesis
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aRNA, Messenger
_xmetabolism
650 0 4 _aRNA-Binding Proteins
650 0 4 _aX Chromosome
700 1 _ade Graaff, E
700 1 _aNg, J
700 1 _aVerkerk, A J
700 1 _aWolfson, S
700 1 _aFisch, G S
700 1 _aKozak, L
700 1 _aNeri, G
700 1 _aOostra, B A
773 0 _tAmerican journal of medical genetics
_gvol. 51
_gno. 4
_gp. 309-14
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320510405
_zAvailable from publisher's website
999 _c7942323
_d7942323