Genomic copy number variation in schizophrenia: rare structural variants as an important source of schizophrenia susceptibility: indications of aetiological overlap with other neurodevelopmental disorders

Andrés Ingason

Genomic copy number variation in schizophrenia: rare structural variants as an important source of schizophrenia susceptibility: indications of aetiological overlap with other neurodevelopmental disorders

Original language	English

Place of Publication	København
Publisher	University of Copenhagen
Number of pages	45
Publication status	Published - 2010

Cite this

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title = "Genomic copy number variation in schizophrenia: rare structural variants as an important source of schizophrenia susceptibility: indications of aetiological overlap with other neurodevelopmental disorders",

author = "Andr{\'e}s Ingason",

year = "2010",

language = "English",

publisher = "University of Copenhagen",

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TY - BOOK

T1 - Genomic copy number variation in schizophrenia

T2 - rare structural variants as an important source of schizophrenia susceptibility: indications of aetiological overlap with other neurodevelopmental disorders

AU - Ingason, Andrés

PY - 2010

Y1 - 2010

M3 - Ph.D. thesis

BT - Genomic copy number variation in schizophrenia

PB - University of Copenhagen

CY - København

ER -