Pages that link to "Q34386102"
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The following pages link to Evidence that a locus for familial high myopia maps to chromosome 18p (Q34386102):
Displaying 50 items.
- Exome sequencing identifies ZNF644 mutations in high myopia (Q21092428) (← links)
- APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans (Q21144730) (← links)
- The COL1A1 gene and high myopia susceptibility in Japanese (Q24308198) (← links)
- Myopia (Q24527196) (← links)
- Mutations in NYX of individuals with high myopia, but without night blindness (Q24653288) (← links)
- Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia (Q24800149) (← links)
- A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1 (Q28751780) (← links)
- Novel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP) genes in high myopia. (Q30358171) (← links)
- Concise Review: Using Stem Cells to Prevent the Progression of Myopia-A Concept (Q30372541) (← links)
- Methodology and recruitment of probands and their families for the Genes in Myopia (GEM) Study (Q30802371) (← links)
- Pathologic myopia: where are we now?. (Q30870234) (← links)
- Asian Americans: Myopia and Refractive Surgery (Q33194161) (← links)
- Dissecting the genetics of human high myopia: a molecular biologic approach (Q33212530) (← links)
- laminin alpha 1 gene is essential for normal lens development in zebrafish (Q33235707) (← links)
- Association of lumican gene with susceptibility to pathological myopia in the northern han ethnic chinese (Q33720745) (← links)
- Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation (Q33748218) (← links)
- Association analysis of retinoic acid receptor beta (RARbeta) gene with high myopia in Chinese subjects. (Q33869193) (← links)
- Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12 (Q33910053) (← links)
- Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study (Q33914538) (← links)
- Animal Models of Myopia: Learning How Vision Controls the Size of the Eye. (Q33942573) (← links)
- 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 (Q33998544) (← links)
- Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population (Q34208132) (← links)
- Associations of high myopia in childhood (Q34229188) (← links)
- Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family (Q34248573) (← links)
- Exome sequencing reveals CCDC111 mutation associated with high myopia (Q34338729) (← links)
- A second locus for familial high myopia maps to chromosome 12q (Q34387777) (← links)
- High heritability of myopia does not preclude rapid changes in prevalence (Q34636737) (← links)
- Heritability and familial aggregation of refractive error in the Old Order Amish (Q34667896) (← links)
- Nature and nurture: the complex genetics of myopia and refractive error (Q34679031) (← links)
- Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese (Q34700654) (← links)
- The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia. (Q34882604) (← links)
- Heritability of refractive error and familial aggregation of myopia in an elderly American population (Q34975204) (← links)
- Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15. (Q34989383) (← links)
- Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis (Q35068023) (← links)
- Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36. (Q35070567) (← links)
- Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing (Q35221170) (← links)
- Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study (Q35221419) (← links)
- Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations (Q35221649) (← links)
- Current gene discovery strategies for ocular conditions (Q35247767) (← links)
- IGF-1 gene polymorphisms in Polish families with high-grade myopia (Q35255077) (← links)
- Myopia in Singapore: taking a public health approach (Q35319613) (← links)
- The biological basis of myopic refractive error (Q35586346) (← links)
- A synopsis of the prevalence rates and environmental risk factors for myopia (Q35586352) (← links)
- Unilateral high myopia: optical components, associated factors, and visual outcomes (Q35591319) (← links)
- Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies (Q35629086) (← links)
- A comparison of refractive development between two subspecies of infant rhesus monkeys (Macaca mulatta) (Q38634721) (← links)
- Enlargement of the Axial Length and Altered Ultrastructural Features of the Sclera in a Mutant Lumican Transgenic Mouse Model (Q36155357) (← links)
- Familial aggregation of myopia in the Tehran eye study: estimation of the sibling and parent offspring recurrence risk ratios (Q36172083) (← links)
- Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia (Q36408718) (← links)
- Evaluation of MMP2 as a candidate gene for high myopia. (Q36574132) (← links)