The genetic causes of mental retardation in Estonia: fragile X syndrome and creatine transporter defect

The present study was initiated to characterize two most common X-linked MR disorders: fragile X syndrome (FXS) and creatine transporter deficiency in Estonia. Within years 1997 to 2006 in the Department of Genetics of United Laboratories of Tartu University Hospital there were 676 patients (516 chi...

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Bibliographische Detailangaben

Hauptverfasser:	Puusepp, Helen, Carpenter, Helen
Format:	Dissertation
Sprache:	eng ; est
Schlagworte:	dissertatsioonid ETD
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