Identification of novel suggestive loci for high-grade myopia in polish families

Molecular Vision

Volumn 17, Issue , 2011, Pages 2028-2039

  Rydzanicz, Malgorzata ^a   Nath, Swapan K ^b   Sun, Celi ^b   Podfigurna Musielak, Monika ^c   Frajdenberg, Agata ^d,e,f   Mrugacz, Malgorzata ^g   Winters, Daniel ^h   Ratnamala, Uppala ⁱ   Radhakrishna, Uppala ⁱ   Bejjani, Bassem A ^j   Gajecka, Marzena ^a,k  

^a INSTITUTE OF HUMAN GENETICS   (Poland)

^b OKLAHOMA MEDICAL RESEARCH FOUNDATION   (United States)

^c Leszno Hospital   (Poland)

^d POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^e Namsos Hospital   (Norway)

^f LINKÖPING UNIVERSITY HOSPITAL   (Sweden)

^g MEDICAL UNIVERSITY OF BIALYSTOK   (Poland)

^h WASHINGTON STATE UNIVERSITY   (United States)

ⁱ UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^j Signature Genomic Laboratories LLC   (United States)

^k WWAMI   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME 12P; CHROMOSOME 7P; CONTROLLED STUDY; EYE EXAMINATION; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ANALYSIS; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MYOPIA; POLAND; PRESCHOOL CHILD; PRIORITY JOURNAL; REFRACTION ERROR; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 7; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENE EXPRESSION PROFILING; GENETIC LINKAGE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LOD SCORE; MICROSATELLITE REPEATS; MYOPIA; PEDIGREE; POLAND; POLYMORPHISM, SINGLE NUCLEOTIDE; SEVERITY OF ILLNESS INDEX;

EID: 79961243101     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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