000 01410 a2200421 4500
005 20250514231207.0
264 0 _c20050914
008 200509s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.30807
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFan, Hongxin
245 0 0 _aMosaicism for an FMR1 gene deletion in a fragile X female.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cJul 2005
300 _a214-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aBase Sequence
650 0 4 _aBlotting, Southern
650 0 4 _aChild, Preschool
650 0 4 _aDNA
_xchemistry
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFemale
650 0 4 _aFragile X Mental Retardation Protein
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aMolecular Sequence Data
650 0 4 _aMosaicism
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aRNA-Binding Proteins
_xgenetics
700 1 _aBooker, Jessica K
700 1 _aMcCandless, Shawn E
700 1 _aShashi, Vandana
700 1 _aFleming, Alison
700 1 _aFarber, Rosann A
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 136
_gno. 2
_gp. 214-7
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.30807
_zAvailable from publisher's website
999 _c15600774
_d15600774