| 000 | 01165 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250513201945.0 | ||
| 264 | 0 | _c20000224 | |
| 008 | 200002s 0 0 eng d | ||
| 022 | _a1059-7794 | ||
| 024 | 7 |
_a10.1002/(SICI)1098-1004(200002)15:2<135::AID-HUMU2>3.0.CO;2-H _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGirodon-Boulandet, E | |
| 245 | 0 | 0 |
_aScreening practices for mutations in the CFTR gene ABCC7. _h[electronic resource] |
| 260 |
_bHuman mutation _c2000 |
||
| 300 |
_a135-49 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aCystic Fibrosis _xdiagnosis |
| 650 | 0 | 4 |
_aCystic Fibrosis Transmembrane Conductance Regulator _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aGenetic Counseling |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 700 | 1 | _aCazeneuve, C | |
| 700 | 1 | _aGoossens, M | |
| 773 | 0 |
_tHuman mutation _gvol. 15 _gno. 2 _gp. 135-49 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(SICI)1098-1004(200002)15:2<135::AID-HUMU2>3.0.CO;2-H _zAvailable from publisher's website |
| 999 |
_c10604535 _d10604535 |
||