Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis

Ophthalmic Genetics

Volumn 22, Issue 2, 2001, Pages 69-75

  Young, T L ^a   Atwood, L D ^a   Ronan, S M ^a   Dewan, A T ^a   Alvear, A B ^a   Peterson, J ^a   Holleschau, A ^a   King, R A ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

Autosomal dominant high myopia; Disequilibrium testing; Ene mapping

Indexed keywords

ALLELE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 18P; CHROMOSOME MARKER; CONTROLLED STUDY; ETHNIC GROUP; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC HETEROGENEITY; HIGH MYOPIA; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; STATISTICAL ANALYSIS; TELOMERE;

CHROMOSOMES, HUMAN, PAIR 18; GENES, DOMINANT; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MYOPIA; PEDIGREE; PHYSICAL CHROMOSOME MAPPING;

GENETTA; SALVIA;

EID: 0034834260     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/opge.22.2.69.2233     Document Type: Article

References (9)

1. Transmission test for linkage disequilibrium the insulin gene region and insulin-dependent diabetes mellitus
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3. Evidence that a locus for familial high myopia maps to chromosome 18p
4. Exact multi-point quantitative-trait linkage analysis in pedigrees by variance components
5. Linkage disequilibrium mapping of the cornea plana congenita gene CNA2
6. The TDT and other family-based tests for linkage disequilibrium and association
7. Replication of linkage studies of complex traits: An estimation of variation in location estimates
8. Combinatorial mismatch screening (CMS) detects identity by descent (IBD) in small samples of probands and controls from the same Mendelian breeding units