A 3.2Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	European journal of human genetics : EJHG 2008-03, Vol.16 (3), p.312-319
Hauptverfasser:	GILLING, Mette, LAURITSEN, Marlene Briciet, ROSENBERG, Thomas, BRØNDUM-NIELSEN, Karen, COTTERILL, Rodney M. J, LUNDSTEEN, Claes, ROJERS, Hans-Hilger, ULLMANN, Reinhard, BACHE, Iben, TÜMER, Zeynep, TOMMERUP, Niels, MØLLER, Morten, HENRIKSEN, Karen Friis, VICENTE, Astrid, OLIVEIRA, Guiomar, CINTIN, Christina, EIBERG, Hans, ANDERSEN, Paal Skyt, MORS, Ole
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Child clinical studies Developmental disorders Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling Genetics of eukaryotes. Biological and molecular evolution Infantile autism Medical genetics Medical sciences Molecular and cellular biology Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!