000 01722 a2200505 4500
005 20250513061341.0
264 0 _c19930809
008 199308s 0 0 eng d
022 _a0002-9297
040 _aNLM
_beng
_cNLM
100 1 _aKwiatkowski, T J
245 0 0 _aThe gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cAug 1993
300 _a391-400 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aBase Sequence
650 0 4 _aCentromere
650 0 4 _aChild
650 0 4 _aChromosome Mapping
_xmethods
650 0 4 _aChromosomes, Human, Pair 6
650 0 4 _aCloning, Molecular
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Markers
650 0 4 _aHumans
650 0 4 _aLod Score
650 0 4 _aMolecular Sequence Data
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aRecombination, Genetic
650 0 4 _aRepetitive Sequences, Nucleic Acid
650 0 4 _aSequence Analysis, DNA
650 0 4 _aSpinocerebellar Degenerations
_xgenetics
700 1 _aOrr, H T
700 1 _aBanfi, S
700 1 _aMcCall, A E
700 1 _aJodice, C
700 1 _aPersichetti, F
700 1 _aNovelletto, A
700 1 _aLeBorgne-DeMarquoy, F
700 1 _aDuvick, L A
700 1 _aFrontali, M
773 0 _tAmerican journal of human genetics
_gvol. 53
_gno. 2
_gp. 391-400
999 _c8100364
_d8100364