000 | 01360 a2200445 4500 | ||
---|---|---|---|
005 | 20250511230223.0 | ||
264 | 0 | _c19901121 | |
008 | 199011s 0 0 eng d | ||
022 | _a0009-9147 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHighsmith, W E | |
245 | 0 | 0 |
_aFrequency of the delta Phe508 mutation and correlation with XV.2c/KM-19 haplotypes in an American population of cystic fibrosis patients: results of a collaborative study. _h[electronic resource] |
260 |
_bClinical chemistry _cOct 1990 |
||
300 |
_a1741-6 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aCystic Fibrosis _xgenetics |
650 | 0 | 4 | _aGenetic Carrier Screening |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aNucleic Acid Probes |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aPhenylalanine _xdeficiency |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 | _aRisk |
700 | 1 | _aChong, G L | |
700 | 1 | _aOrr, H T | |
700 | 1 | _aPerry, T R | |
700 | 1 | _aSchald, D | |
700 | 1 | _aFarber, R | |
700 | 1 | _aWagner, K | |
700 | 1 | _aKnowles, M R | |
700 | 1 | _aWarwick, W J | |
700 | 1 | _aSilverman, L M | |
773 | 0 |
_tClinical chemistry _gvol. 36 _gno. 10 _gp. 1741-6 |
|
999 |
_c2214771 _d2214771 |