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