000 01490 a2200433 4500
005 20250512023328.0
264 0 _c19870120
008 198701s 0 0 eng d
022 _a0340-6717
024 7 _a10.1007/BF00282546
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aShaw, D J
245 0 0 _aLinkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.
_h[electronic resource]
260 _bHuman genetics
_cNov 1986
300 _a267-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aApolipoprotein C-II
650 0 4 _aApolipoproteins C
_xgenetics
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 19
650 0 4 _aComplement C3
_xgenetics
650 0 4 _aDNA
_xgenetics
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Markers
650 0 4 _aHumans
650 0 4 _aMyotonic Dystrophy
_xgenetics
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aReceptor, Insulin
_xgenetics
650 0 4 _aReceptors, LDL
_xgenetics
700 1 _aMeredith, A L
700 1 _aBrook, J D
700 1 _aSarfarzi, M
700 1 _aHarley, H G
700 1 _aHuson, S M
700 1 _aBell, G I
700 1 _aHarper, P S
773 0 _tHuman genetics
_gvol. 74
_gno. 3
_gp. 267-9
856 4 0 _uhttps://doi.org/10.1007/BF00282546
_zAvailable from publisher's website
999 _c2883780
_d2883780