| 000 | 01691 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250515191822.0 | ||
| 264 | 0 | _c20100719 | |
| 008 | 201007s 0 0 eng d | ||
| 022 | _a1096-1194 | ||
| 024 | 7 |
_a10.1016/j.mcp.2009.10.006 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGrasso, Marina | |
| 245 | 0 | 0 |
_aThe -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotype. _h[electronic resource] |
| 260 |
_bMolecular and cellular probes _cApr 2010 |
||
| 300 |
_a107-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAged, 80 and over |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFragile X Mental Retardation Protein _xgenetics |
| 650 | 0 | 4 |
_aFragile X Syndrome _xgenetics |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPromoter Regions, Genetic _xgenetics |
| 700 | 1 | _aCecconi, Massimiliano | |
| 700 | 1 | _aBoni, Stefania | |
| 700 | 1 | _aForzano, Francesca | |
| 700 | 1 | _aBarbaresi, Maurizio | |
| 700 | 1 | _aMemo, Luigi | |
| 700 | 1 | _aPerroni, Lucia | |
| 700 | 1 | _aFaravelli, Francesca | |
| 700 | 1 | _aDi Maria, Emilio | |
| 773 | 0 |
_tMolecular and cellular probes _gvol. 24 _gno. 2 _gp. 107-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.mcp.2009.10.006 _zAvailable from publisher's website |
| 999 |
_c19228449 _d19228449 |
||