Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination.
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DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype CorrelationsAn Alu transposition model for the origin and expansion of human segmental duplications.Unequal exchange and meiotic instability of disease-resistance genes in the Rp1 region of maize.Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2.Topoisomerase I and II consensus sequences in a 17-kb deletion junction of the COL4A5 and COL4A6 genes and immunohistochemical analysis of esophageal leiomyomatosis associated with Alport syndrome.MLPA-based genotype-phenotype analysis in 1053 Chinese patients with DMD/BMD.Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndromeApolipoprotein(a) gene accounts for greater than 90% of the variation in plasma lipoprotein(a) concentrationsExon duplications in the ATP7A gene: frequency and transcriptional behaviour.Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.Alu-Alu recombination results in a duplication of seven exons in the lysyl hydroxylase gene in a patient with the type VI variant of Ehlers-Danlos syndromeThe transposon-driven evolutionary origin and basis of histone deacetylase functions and limitations in disease prevention.Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and femalesDuchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large CohortIntegration of a vector containing a repetitive LINE-1 element in the human genome.
P2860
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P2860
Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Mechanisms of tandem duplicati ...... ntrachromosomal recombination.
@en
type
label
Mechanisms of tandem duplicati ...... ntrachromosomal recombination.
@en
prefLabel
Mechanisms of tandem duplicati ...... ntrachromosomal recombination.
@en
P2093
P2860
P1433
P1476
Mechanisms of tandem duplicati ...... ntrachromosomal recombination.
@en
P2093
P2860
P304
P407
P577
1991-09-01T00:00:00Z