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1. ESICM LIVES 2016: part one: Milan, Italy. 1-5 October 2016

2. Expanding the range of ZNF804A variants conferring risk of psychosis

3. Copy number variations of chromosome 16p13.1 region associated with schizophrenia

4. Meta-analysis of 32 genome-wide linkage studies of schizophrenia

10. Abstract PR575

11. Abstract PR051

12. Abstract PR022

13. Disruption of the neurexin 1 gene is associated with schizophrenia

14. Common variants conferring risk of schizophrenia

15. Large recurrent microdeletions associated with schizophrenia

16. Large recurrent microdeletions associated with schizophrenia [Letter to Nature]

17. Distribution of symptom dimensions across Kraepelinian divisions

19. Copy number variations of chromosome 16p13.1 region associated with schizophrenia

20. Expanding the range of ZNF804A variants conferring risk of psychosis

21. Neuregulin-1 genotypes and eye movements in schizophrenia

22. Disruption of the neurexin 1 gene is associated with schizophrenia.

23. Large recurrent microdeletions associated with schizophrenia.

24. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study

40. New DNA markers with increased informativeness show diminished support for a chromosome 5q11–13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families

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