| 000 | 01357 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250514194107.0 | ||
| 264 | 0 | _c20050218 | |
| 008 | 200502s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.30199 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aChassaing, N | |
| 245 | 0 | 0 |
_aMolecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cAug 2004 |
||
| 300 |
_a410-3 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 2 |
| 650 | 0 | 4 | _aCytogenetic Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFibrous Dysplasia, Polyostotic _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMicrosatellite Repeats |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 700 | 1 | _aDe Mas, P | |
| 700 | 1 | _aTauber, M | |
| 700 | 1 | _aVincent, M C | |
| 700 | 1 | _aJulia, S | |
| 700 | 1 | _aBourrouillou, G | |
| 700 | 1 | _aCalvas, P | |
| 700 | 1 | _aBieth, E | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 128A _gno. 4 _gp. 410-3 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.30199 _zAvailable from publisher's website |
| 999 |
_c14966601 _d14966601 |
||