A novel locus for congenital simple microphthalmia family mapping to 17p12-q12

Investigative Ophthalmology and Visual Science

Volumn 52, Issue 6, 2011, Pages 3425-3429

  Hu, Zhengmao ^a   Yu, Changhong ^a,b,c   Li, Jingzhi ^a   Wang, Yiqiang ^b   Liu, Deyuan ^a   Xiang, Xinying ^a   Su, Wei ^a   Pan, Qian ^a   Xie, Lixin ^b   Xia, Kun ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b SHANDONG EYE INSTITUTE   (China)

^c QINGDAO UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

FRUCTOSE BISPHOSPHATE ALDOLASE; MEDIATOR COMPLEX; MEDIATOR COMPLEX 9; MICROSATELLITE DNA; MONOCYTE CHEMOTACTIC PROTEIN 2; PROTEIN SERINE THREONINE KINASE; RECEPTOR INTERACTING PROTEIN 140; RIBOSOME PROTEIN; SPERM ANTIGEN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHINESE; CHROMOSOME 17; CLINICAL ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENOTYPING TECHNIQUE; HAPLOTYPE; HUMAN; MALE; MICROPHTHALMIA; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; CHROMOSOME MAP; GENETIC ASSOCIATION; GENETICS; GENOTYPE; PEDIGREE; POLYMERASE CHAIN REACTION;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENETIC LINKAGE; GENETIC LOCI; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LOD SCORE; MALE; MICROPHTHALMOS; MICROSATELLITE REPEATS; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 80051557361     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-6747     Document Type: Article

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