Association studies in consanguineous populations

American Journal of Human Genetics

Volumn 58, Issue 4, 1996, Pages 861-866

  Génin, Emmanuelle ^a,b   Clerget Darpoux, Françoise ^a  

^a INSTITUT NATIONAL D'ÉTUDES DÉMOGRAPHIQUES   (France)

^b INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONSANGUINITY; DISEASE PREDISPOSITION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; INBREEDING; INHERITANCE; MARKER GENE; MULTIFACTORIAL GENETIC DISORDER; PRIORITY JOURNAL;

CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; CONSANGUINITY; DISEASE SUSCEPTIBILITY; FEMALE; GENE FREQUENCY; GENETIC DISEASES, INBORN; GENETIC MARKERS; GENETICS, POPULATION; GENOTYPE; HUMANS; LINKAGE (GENETICS); MALE; PROBABILITY;

EID: 0029865414     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

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2. Lander ES, Botstein D (1987) Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science 236:1567-1570
3. Lander ES, Schork NJ (1994). Genetic dissection of complex traits. Science 265:2037-2048
4. Pollack MR, Wu Chou YH, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE (1993) Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Nat Genet 5:201-204
5. Thomson G (1983) Investigation of the mode of inheritance of the HLA associated diseases by the method of antigen genotype frequencies among diseased individuals. Tissue Antigens 21:81-104