000 01487 a2200373 4500
005 20250513175502.0
264 0 _c19990610
008 199906s 0 0 eng d
022 _a1059-7794
024 7 _a10.1002/(SICI)1098-1004(1999)13:4<318::AID-HUMU9>3.0.CO;2-F
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLarsen, L A
245 0 0 _aHigh-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants.
_h[electronic resource]
260 _bHuman mutation
_c1999
300 _a318-27 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aCardiomyopathy, Hypertrophic
_xgenetics
650 0 4 _aDNA Mutational Analysis
_xinstrumentation
650 0 4 _aElectrophoresis, Capillary
_xinstrumentation
650 0 4 _aHumans
650 0 4 _aLong QT Syndrome
_xgenetics
650 0 4 _aPoint Mutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Genetic
650 0 4 _aPolymorphism, Single-Stranded Conformational
650 0 4 _aSequence Analysis, DNA
650 0 4 _aTemperature
700 1 _aChristiansen, M
700 1 _aVuust, J
700 1 _aAndersen, P S
773 0 _tHuman mutation
_gvol. 13
_gno. 4
_gp. 318-27
856 4 0 _uhttps://doi.org/10.1002/(SICI)1098-1004(1999)13:4<318::AID-HUMU9>3.0.CO;2-F
_zAvailable from publisher's website
999 _c10179314
_d10179314