000 01713 a2200481 4500
005 20250514185914.0
264 0 _c20041119
008 200411s 0 0 eng d
022 _a0001-5652
024 7 _a10.1159/000077385
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBartlett, Christopher W
245 0 0 _aExamination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.
_h[electronic resource]
260 _bHuman heredity
_c2004
300 _a10-20 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 _aAutistic Disorder
_xgenetics
650 0 4 _aCanada
650 0 4 _aChromosomes, Human, Pair 13
650 0 4 _aChromosomes, Human, Pair 2
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aCommunication Disorders
_xgenetics
650 0 4 _aCystic Fibrosis Transmembrane Conductance Regulator
_xgenetics
650 0 4 _aGenetic Linkage
650 0 4 _aGenetic Markers
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aLanguage Disorders
_xgenetics
650 0 4 _aLinkage Disequilibrium
650 0 4 _aLod Score
650 0 4 _aModels, Genetic
650 0 4 _aPhenotype
650 0 4 _aStatistics as Topic
_xmethods
650 0 4 _aUnited States
700 1 _aFlax, Judy F
700 1 _aLogue, Mark W
700 1 _aSmith, Brett J
700 1 _aVieland, Veronica J
700 1 _aTallal, Paula
700 1 _aBrzustowicz, Linda M
773 0 _tHuman heredity
_gvol. 57
_gno. 1
_gp. 10-20
856 4 0 _uhttps://doi.org/10.1159/000077385
_zAvailable from publisher's website
999 _c14842978
_d14842978