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Volumn 21, Issue 4, 2011, Pages 173-182

Strategies to identify genes for complex disorders: A focus on bipolar disorder and chromosome 16p

Author keywords

association analysis; bipolar disorder; chromosome 16; genetics; linkage analysis; manic depression; sequencing

Indexed keywords

ALLELE; BIPOLAR DISORDER; BRAIN FUNCTION; CHROMOSOME 12Q; CHROMOSOME 13Q; CHROMOSOME 14; CHROMOSOME 16P; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME 20Q; CHROMOSOME 21Q; CHROMOSOME 4P; CHROMOSOME 4Q; CHROMOSOME 5Q; CHROMOSOME 6Q; CHROMOSOME 8Q; CHROMOSOME 9Q; CHROMOSOME REPLICATION; CHROMOSOME XQ; CODON; COPY NUMBER VARIATION; COST EFFECTIVENESS ANALYSIS; DIAGNOSTIC ERROR; DISEASE PREDISPOSITION; DNA POLYMORPHISM; DNA SEQUENCE; EXON; FALSE POSITIVE RESULT; GENE DELETION; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC VARIABILITY; GENOTYPE; HUMAN; IN VITRO STUDY; IN VIVO STUDY; LIMIT OF DETECTION; META ANALYSIS (TOPIC); NERVE CELL DIFFERENTIATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79960364274     PISSN: 09558829     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0b013e32833a21e3     Document Type: Review
Times cited : (6)

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