000 01545 a2200481 4500
005 20250513215218.0
264 0 _c20000919
008 200009s 0 0 eng d
022 _a0002-9297
024 7 _a10.1086/303039
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRoss, J L
245 0 0 _aThe Turner syndrome-associated neurocognitive phenotype maps to distal Xp.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cSep 2000
300 _a672-81 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aBody Height
_xgenetics
650 0 4 _aChild
650 0 4 _aChromosome Breakage
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Mapping
650 0 4 _aDosage Compensation, Genetic
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aMiddle Aged
650 0 4 _aMosaicism
_xgenetics
650 0 4 _aOvary
_xphysiopathology
650 0 4 _aPhenotype
650 0 4 _aSpace Perception
_xphysiology
650 0 4 _aTurner Syndrome
_xgenetics
650 0 4 _aVisual Perception
_xgenetics
650 0 4 _aX Chromosome
_xgenetics
700 1 _aRoeltgen, D
700 1 _aKushner, H
700 1 _aWei, F
700 1 _aZinn, A R
773 0 _tAmerican journal of human genetics
_gvol. 67
_gno. 3
_gp. 672-81
856 4 0 _uhttps://doi.org/10.1086/303039
_zAvailable from publisher's website
999 _c10880702
_d10880702