000 01225 a2200361 4500
005 20250517160833.0
264 0 _c20190730
008 201907s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/cge.13075
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMila, M
245 0 0 _aFragile X syndrome: An overview and update of the FMR1 gene.
_h[electronic resource]
260 _bClinical genetics
_c02 2018
300 _a197-205 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAtaxia
_xgenetics
650 0 4 _aAutistic Disorder
_xgenetics
650 0 4 _aFemale
650 0 4 _aFragile X Mental Retardation Protein
_xgenetics
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aPrimary Ovarian Insufficiency
_xgenetics
650 0 4 _aTremor
_xgenetics
700 1 _aAlvarez-Mora, M I
700 1 _aMadrigal, I
700 1 _aRodriguez-Revenga, L
773 0 _tClinical genetics
_gvol. 93
_gno. 2
_gp. 197-205
856 4 0 _uhttps://doi.org/10.1111/cge.13075
_zAvailable from publisher's website
999 _c27280752
_d27280752