Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping

Journal of Physiology

Volumn 554, Issue 1, 2004, Pages 40-45

  Broeckel, Ulrich ^a   Schork, Nicholas J ^b  

^a MEDICAL COLLEGE OF WISCONSIN   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ENVIRONMENTAL FACTOR; GENE FUNCTION; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC LINKAGE; GENETIC RECOMBINATION; GENETIC VARIABILITY; HAPLOTYPE; HEREDITY; HERITABILITY; HUMAN; HUMAN GENETICS; MEDICAL RESEARCH; MEIOSIS; MOLECULAR BIOLOGY; PHENOTYPIC VARIATION; PRIORITY JOURNAL; REVIEW; DNA MARKER; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PROCEDURES; GENETIC SUSCEPTIBILITY; HAPLOTYPE MAP; HUMAN GENOME; HYPERTENSION; MONOGENIC DISORDER; PEDIGREE; PHENOTYPE; PHYLOGENY; RECOMBINATION MAPPING;

CHROMOSOME MAPPING; GENETIC DISEASES, INBORN; HUMANS; PHENOTYPE; RECOMBINATION, GENETIC; VARIATION (GENETICS);

EID: 0348184970     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1113/jphysiol.2003.051128     Document Type: Review

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