000 01344 a2200433 4500
005 20250511193952.0
264 0 _c19920716
008 199207s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320430142
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMalmgren, H
245 0 0 _aMethylation and mutation patterns in the fragile X syndrome.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_c
300 _a268-78 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA Probes
650 0 4 _aDiseases in Twins
_xgenetics
650 0 4 _aFemale
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMethylation
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aTwins, Monozygotic
700 1 _aSteén-Bondeson, M L
700 1 _aGustavson, K H
700 1 _aSeémanova, E
700 1 _aHolmgren, G
700 1 _aOberlé, I
700 1 _aMandel, J L
700 1 _aPettersson, U
700 1 _aDahl, N
773 0 _tAmerican journal of medical genetics
_gvol. 43
_gno. 1-2
_gp. 268-78
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320430142
_zAvailable from publisher's website
999 _c1611689
_d1611689