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 |