Analysis of 22 deletion breakpoints in dystrophin intron 49.
about
Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypesMechanisms of change in gene copy numberA microhomology-mediated break-induced replication model for the origin of human copy number variation.Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell linesCopy number variation in human health, disease, and evolution.Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients.Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.Complex genomic rearrangements in the dystrophin gene due to replication-based mechanisms.On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.Becker muscular dystrophy due to an inversion of exons 23 and 24 of the DMD gene.Mechanisms for human genomic rearrangementsIonising radiation and genetic risks. XVI. A genome-based framework for risk estimation in the light of recent advances in genome research.Decoding NF1 Intragenic Copy-Number Variations.Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene.Sequence analysis of 17 NRXN1 deletions.Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms.
P2860
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P2860
Analysis of 22 deletion breakpoints in dystrophin intron 49.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@en
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@nl
type
label
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@en
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@nl
prefLabel
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@en
Analysis of 22 deletion breakpoints in dystrophin intron 49.
@nl
P2093
P50
P1433
P1476
Analysis of 22 deletion breakpoints in dystrophin intron 49
@en
P2093
Barbara Cardazzo
Carlo Nobile
Francesca Rizzi
Gian Antonio Danieli
Luisa Toffolatti
P2888
P304
P356
10.1007/S00439-002-0721-7
P577
2002-04-09T00:00:00Z