Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12
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APLP2 Regulates Refractive Error and Myopia Development in Mice and HumansA genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1Automatic diagnosis of pathological myopia from heterogeneous biomedical dataMethodology and recruitment of probands and their families for the Genes in Myopia (GEM) Study.Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family StudyGenome-wide scan of African-American and white families for linkage to myopia.Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family.Association of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus.The effect of two-zone concentric bifocal spectacle lenses on refractive error development and eye growth in young chicks.Heritability and familial aggregation of refractive error in the Old Order Amish.Nature and nurture: the complex genetics of myopia and refractive error.Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi familiesHeritability of refractive error and familial aggregation of myopia in an elderly American populationGenomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15.Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis.Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36.Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family.NYX mutations in four families with high myopia with or without CSNB1Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study.Current gene discovery strategies for ocular conditionsReplication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies.Genetic variants near PDGFRA are associated with corneal curvature in Australians.Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia.Evaluation of MMP2 as a candidate gene for high myopia.An international collaborative family-based whole-genome linkage scan for high-grade myopiaA review of current approaches to identifying human genes involved in myopia.Molecular genetics of human myopia: an update.Linkage analysis of high myopia susceptibility locus in 26 familiesMyopia genetics: a review of current research and emerging trends.Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese populationCommon variant in myocilin gene is associated with high myopia in isolated population of Korcula Island, Croatia.Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12Lack of association with high myopia and the MYP2 locus in the Japanese population by high resolution microsatellite analysis on chromosome 18.Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36.The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures.Genetic isolates in ophthalmic diseases.Heritability analysis of spherical equivalent, axial length, corneal curvature, and anterior chamber depth in the Beaver Dam Eye Study
P2860
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P2860
Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12
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2004 nî lūn-bûn
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2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2004年の論文
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2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@ast
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@en
type
label
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@ast
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@en
prefLabel
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@ast
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@en
P2093
P2860
P356
P1476
Genomewide linkage scan for my ...... of linkage on chromosome 22q12
@en
P2093
Debra Dana
Elise Ciner
Grace Ibay
Lauren Reider
Melissa Schlifka
Taura Holmes
P2860
P304
P356
10.1086/423789
P407
P577
2004-07-23T00:00:00Z