| 000 | 01374 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250518024653.0 | ||
| 264 | 0 | _c20200619 | |
| 008 | 202006s 0 0 eng d | ||
| 022 | _a1741-4520 | ||
| 024 | 7 |
_a10.1111/cga.12331 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aShahid, Muhammad | |
| 245 | 0 | 0 |
_aScreening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations. _h[electronic resource] |
| 260 |
_bCongenital anomalies _cJan 2020 |
||
| 300 |
_a32-39 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aFanconi Anemia _xepidemiology |
| 650 | 0 | 4 |
_aFanconi Anemia Complementation Group A Protein _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntrons _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aPakistan _xepidemiology |
| 700 | 1 | _aFirasat, Sabika | |
| 700 | 1 | _aSatti, Humayoon Shafique | |
| 700 | 1 | _aSatti, Tariq Mahmood | |
| 700 | 1 | _aGhafoor, Tariq | |
| 700 | 1 | _aSharif, Imtenan | |
| 700 | 1 | _aAfshan, Kiran | |
| 773 | 0 |
_tCongenital anomalies _gvol. 60 _gno. 1 _gp. 32-39 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/cga.12331 _zAvailable from publisher's website |
| 999 |
_c29417436 _d29417436 |
||