000 02505 a2200829 4500
005 20250516204901.0
264 0 _c20140530
008 201405s 0 0 eng d
022 _a1537-6605
024 7 _a10.1016/j.ajhg.2014.03.007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAl Turki, Saeed
245 0 0 _aRare variants in NR2F2 cause congenital heart defects in humans.
_h[electronic resource]
260 _bAmerican journal of human genetics
_c04 2014
300 _a574-85 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aBinding Sites
650 0 4 _aCOUP Transcription Factor II
_xgenetics
650 0 4 _aCell Line
650 0 4 _aExome
650 0 4 _aFemale
650 0 4 _aHeart Defects, Congenital
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMice
650 0 4 _aMutation, Missense
650 0 4 _aPedigree
650 0 4 _aProspective Studies
650 0 4 _aTranscription, Genetic
700 1 _aManickaraj, Ashok K
700 1 _aMercer, Catherine L
700 1 _aGerety, Sebastian S
700 1 _aHitz, Marc-Phillip
700 1 _aLindsay, Sarah
700 1 _aD'Alessandro, Lisa C A
700 1 _aSwaminathan, G Jawahar
700 1 _aBentham, Jamie
700 1 _aArndt, Anne-Karin
700 1 _aLouw, Jacoba
700 1 _aLow, Jacoba
700 1 _aBreckpot, Jeroen
700 1 _aGewillig, Marc
700 1 _aThienpont, Bernard
700 1 _aAbdul-Khaliq, Hashim
700 1 _aHarnack, Christine
700 1 _aHoff, Kirstin
700 1 _aKramer, Hans-Heiner
700 1 _aSchubert, Stephan
700 1 _aSiebert, Reiner
700 1 _aToka, Okan
700 1 _aCosgrove, Catherine
700 1 _aWatkins, Hugh
700 1 _aLucassen, Anneke M
700 1 _aO'Kelly, Ita M
700 1 _aSalmon, Anthony P
700 1 _aBu'lock, Frances A
700 1 _aGranados-Riveron, Javier
700 1 _aSetchfield, Kerry
700 1 _aThornborough, Chris
700 1 _aBrook, J David
700 1 _aMulder, Barbara
700 1 _aKlaassen, Sabine
700 1 _aBhattacharya, Shoumo
700 1 _aDevriendt, Koen
700 1 _aFitzpatrick, David F
700 1 _aWilson, David I
700 1 _aMital, Seema
700 1 _aHurles, Matthew E
773 0 _tAmerican journal of human genetics
_gvol. 94
_gno. 4
_gp. 574-85
856 4 0 _uhttps://doi.org/10.1016/j.ajhg.2014.03.007
_zAvailable from publisher's website
999 _c23709145
_d23709145