Moss, Philip I.
9  Ergebnisse:
Personensuche X
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2

Genetic contributors to risk of schizophrenia in the presen..:

Cleynen I ; Engchuan W ; Hestand M. S...
info:eu-repo/semantics/altIdentifier/pmid/32015465.  , 2020
 
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects w..:

Zhao, Y.J ; Diacou, A ; Johnston, H.R...
Zhao , Y J , Diacou , A , Johnston , H R , Musfee , F I , McDonald-McGinn , D M , McGinn , D , Crowley , T B , Repetto , G M , Swillen , A , Breckpot , J , Vermeesch , J R , Kates , W R , Digilio , M C , Unolt , M , Marino , B , Pontillo , M , Armando , M , Di Fabio , F , Vicari , S , van den Bree , M , Moss , H , Owen , M J , Murphy , K C , Murphy , C M , Murphy , D , Schoch , K , Shashi , V , Tassone , F , Simon , T J , Shprintzen , R J , Campbell , L , Philip , N , Heine-Suner , D , Garcia-Minaur , S , Fernandez , L , Bearden , C E , Vingerhoets , C , van Amelsvoort , T , Eliez , S , Schneider , M , Vorstman , J A S , Gothelf , D , Zackai , E , Agopian , A J , Gur , R E , Bassett , A S , Emanuel , B S , Goldmuntz , E , Mitchell , L E , Wang , T & International 22q11.2 Brain and Behavior Consortium 2020 , ' Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects ' , American Journal of Hu....  , 2020
 
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