Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping

International Journal of Molecular Medicine

Volumn 21, Issue 4, 2008, Pages 429-438

  Nürnberg, Gudrun ^a   Jacobi, Felix K ^b   Broghammer, Martina ^c   Becker, Christian ^a   Blin, Nikolaus ^c   Nürnberg, Peter ^a,d   Stephani, Ulrich ^e   Pusch, Carsten M ^c  

^a UNIVERSITY OF COLOGNE   (Germany)

^b Ambulatory Eye Surgery Center   (Germany)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d UNIVERSITY OF COLOGNE   (Germany)

^e UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

Author keywords

Composite interval; Haplotype analysis; Linkage study; Mendelian inheritance; Microarray; Myopia; Short sightedness; Single nucleotide polymorphism; Whole genome chips

Indexed keywords

GENE PRODUCT; PROTEIN MYP3;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CATARACT; CHILD; CHROMOSOME 12; CHROMOSOME 12Q; CONTROLLED STUDY; DISEASE SEVERITY; ETHNICITY; EYE AXIS LENGTH; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC DATABASE; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION; GENETIC RECOMBINATION; GENETIC SIMILARITY; GERMANY; GLAUCOMA; HUMAN; ITALY; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; MYOPIA; PATHOPHYSIOLOGY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; REFRACTION ERROR; RETINA DETACHMENT; RETINA MACULA DEGENERATION; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; ADOLESCENT; AGED; CHROMOSOME MAP; DEGENERATIVE MYOPIA; DNA MICROARRAY; DOMINANT GENE; GENETIC LINKAGE; GENETICS; HAPLOTYPE; MIDDLE AGED; PEDIGREE;

ADOLESCENT; ADULT; AGED; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; GENES, DOMINANT; GERMANY; HAPLOTYPES; HUMANS; LOD SCORE; MALE; MIDDLE AGED; MYOPIA, DEGENERATIVE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 44649134555     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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