Distinct disorders affecting the brain share common genetic origins

F1000 Biology Reports

Volumn 2, Issue 1, 2010, Pages

  Kooy, R Frank ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CONTACTIN; CONTACTIN ASSOCIATED PROTEIN LIKE 2; NEUREXIN; NEUREXIN 1; UNCLASSIFIED DRUG;

AUTISM; BACTERIAL ARTIFICIAL CHROMOSOME; BRAIN DISEASE; CHROMOSOME 15Q; CHROMOSOME 7Q; CHROMOSOME BREAKAGE; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; COPY NUMBER VARIATION; GENE DELETION; GENE EXPRESSION; GENE FUSION; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC RISK; HAPPY PUPPET SYNDROME; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN GENOME; INTELLIGENCE QUOTIENT; MACROCEPHALY; MENTAL DEFICIENCY; MONOZYGOTIC TWINS; NEUROLOGIC DISEASE; NEUROPSYCHIATRY; PHENOTYPE; REVIEW; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77955069720     PISSN: 17404118     EISSN: 1757594X     Source Type: Journal    
DOI: 10.3410/B2-11     Document Type: Review

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