Evidence that a locus for familial high myopia maps to chromosome 18p - Wikidata - awgldk - TriplyDB

Evidence that a locus for familial high myopia maps to chromosome 18p

Evidence that a locus for familial high myopia maps to chromosome 18p

http://www.wikidata.org/entity/Q34386102

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Exome sequencing identifies ZNF644 mutations in high myopia APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans Myopia.Mutations in NYX of individuals with high myopia, but without night blindness Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1 Concise Review: Using Stem Cells to Prevent the Progression of Myopia-A Concept Methodology and recruitment of probands and their families for the Genes in Myopia (GEM) Study.Dissecting the genetics of human high myopia: a molecular biologic approach laminin alpha 1 gene is essential for normal lens development in zebrafish.Association of lumican gene with susceptibility to pathological myopia in the northern han ethnic chinese Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation.Association analysis of retinoic acid receptor beta (RARbeta) gene with high myopia in Chinese subjects.Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12 Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study Animal Models of Myopia: Learning How Vision Controls the Size of the Eye.A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population Associations of high myopia in childhood.Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family.Exome sequencing reveals CCDC111 mutation associated with high myopia.A second locus for familial high myopia maps to chromosome 12q High heritability of myopia does not preclude rapid changes in prevalence.Heritability and familial aggregation of refractive error in the Old Order Amish.Nature and nurture: the complex genetics of myopia and refractive error.Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia.Heritability of refractive error and familial aggregation of myopia in an elderly American population Genomewide 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.Refinement 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.Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations.Current gene discovery strategies for ocular conditions IGF-1 gene polymorphisms in Polish families with high-grade myopia Myopia in Singapore: taking a public health approach Unilateral high myopia: optical components, associated factors, and visual outcomes Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies.A comparison of refractive development between two subspecies of infant rhesus monkeys (Macaca mulatta)

P2860

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P2860

Evidence that a locus for familial high myopia maps to chromosome 18p

http://www.wikidata.org/entity/Q34386102

description

1998 nî lūn-bûn

@nan

1998 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի հուլիսին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

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1998年論文

@zh-tw

1998年论文

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name

Evidence that a locus for familial high myopia maps to chromosome 18p

@ast

Evidence that a locus for familial high myopia maps to chromosome 18p

@en

Evidence that a locus for familial high myopia maps to chromosome 18p

@nl

type

label

Evidence that a locus for familial high myopia maps to chromosome 18p

@ast

Evidence that a locus for familial high myopia maps to chromosome 18p

@en

Evidence that a locus for familial high myopia maps to chromosome 18p

@nl

prefLabel

Evidence that a locus for familial high myopia maps to chromosome 18p

@ast

Evidence that a locus for familial high myopia maps to chromosome 18p

@en

Evidence that a locus for familial high myopia maps to chromosome 18p

@nl

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P2860

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P1433

American Journal of Human Genetics

P1476

Evidence that a locus for familial high myopia maps to chromosome 18p

@en

P2093

Alvear AB

http://www.w3.org/2001/XMLSchema#string

Atwood LD

http://www.w3.org/2001/XMLSchema#string

Drahozal LA

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King RA

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Oetting WS

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Ronan SM

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Wildenberg SC

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Wilkin DJ

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Young TL

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P2860

Strategies for multilocus linkage analysis in humans

A comprehensive genetic map of the human genome based on 5,264 microsatellites

The 1993-94 Généthon human genetic linkage map

INCIDENCE OF MYOPIA IN CHINA: Data and theses from periodical investigations covering thirty years residence, and association with refracting and hospital centres, in a score of the larger cities.

Easy calculations of lod scores and genetic risks on small computers

Faster sequential genetic linkage computations

An immunoelectron microscope study of the aged human lens capsule.

HEREDITARY ABNORMALITIES OF THE EYE: VII. INHERITABLE DEFECTS INVOLVING EYE MUSCLES, REFRACTION, ETC.

Construction of multilocus genetic linkage maps in humans.

Identification of a gene that causes primary open angle glaucoma.

P304

109-119

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scholarly article

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10.1086/301907

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P407

P433

1

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P478

63

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P577

1998-07-01T00:00:00Z

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13649137

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9634508

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1377231

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