New insights into the biological basis of genomic disorders

Nature Genetics

Volumn 38, Issue 12, 2006, Pages 1363-1364

  Myers, Simon R ^a   McCarroll, Steven A ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; DISEASE ASSOCIATION; DNA DETERMINATION; DNA SEQUENCE; GENE DELETION; GENE DUPLICATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC LINKAGE; GENETIC RECOMBINATION; GENETIC STABILITY; GENOMICS; HUMAN; HUMAN CHROMOSOME; HUMAN GENOME; PRIORITY JOURNAL; SHORT SURVEY;

ALLELES; FEMALE; GENE DELETION; GENE DUPLICATION; GENETIC DISEASES, INBORN; HUMANS; MALE; MEIOSIS; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; SYNDROME;

EID: 33751526542     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1206-1363     Document Type: Short Survey

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