Using a 1-LOD support interval approach, we estimated the size of this region of linkage as 2 Mb and to be bounded by SNPs rs10489254 to rs10494827. Using the same approach, regions of suggestive linkage ((maxNPL)42.2)25 were observed for a 6.5 Mb region of chromosome 14q24.3–q31.1...
(2008a). Comparative chromosome mapping of sex-linked Szymura JM et al. (2003). A linkage map for the hybridising genes and identification of sex chromosomal rearrangements toads Bombina bombina and B. variegata (Anura: Discoglossi- in the Japanese wrinkled frog (Rana rugosa, Ranidae) with...
We have previously reported strong linkage on chromosome 10q in pedigrees transmitting Alzheimer's disease through the mother, overlapping with many significant linkage reports including the largest reported study. Here, we report the most comprehensive fine mapping of this region to date. In a sample...
Chromosome image analysis system ver. 4.0Chromosome mappingFluorescence in situ hybridizationRed clover ( Trifolium pratense L . )Red clover ( Trifolium pratense L.) is a forage legume and an allogamous diploid plant (2n = 14; 440 Mb). Here, we examine the 7 prometaphase chromosomes of red...
Based on combined fluorescencein situhybridization and linkage mapping, the gene order on CFA9 is similar to that of the homologous genes on HSA17q and mouse chromosome 11 (MMU11), but in the dog the gene order is inverted with respect to the centromere. Canine loci, GALK1, TK1, GH1, ...
The genes controlling resistance to three wheat rusts, viz., leaf rust (Lr26), stem rust (Sr31) and stripe or yellow rust (Yr9), and ω-secalins (Sec1), located on the short arm of rye chromosome 1R, were mapped with respect to each other and the centromere. Analysis of 214 seed...
A large linkage group has been assigned to chromosome 19. The loci have been ordered using a two-point mapping analysis based on all available family linkage data summarized in the form of lod score tables. Get PDF (500K) More content like this Find more content: like this article Find...
12-q23.3 region are contributing to the expression of the clinical phenotype and the strongest evidence for linkage is in a region near the gene encoding and (2) a susceptibility locus for both and maps to this region. 展开 关键词: Asthma Chromosome Mapping Chromosomes, Human, Pair 12 ...
Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25 Contributors M-CT is the main author of this report. M-CT, Y-JC, J-TC and D-WL conducted the bibliographical search and coordination of the discussion...
Mapping of Reis–Bücklers' corneal dystrophy to chromosome 5q Am. J. Ophthalmol. (1996) E. Heon Linkage of posterior polymorphous corneal dystrophy to 20q11 Hum. Mol. Genet. (1995) A.D. Irvine Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy Nature ...