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SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints
by
Vogt, Julia
,
Bengesser, Kathrin
,
Claes, Kathleen B M
,
Wimmer, Katharina
,
Mautner, Victor-Felix
,
van Minkelen, Rick
,
Legius, Eric
,
Brems, Hilde
,
Upadhyaya, Meena
,
Högel, Josef
,
Lazaro, Conxi
,
Rosenbaum, Thorsten
,
Bammert, Simone
,
Messiaen, Ludwine
,
Cooper, David N
,
Kehrer-Sawatzki, Hildegard
Published in
Genome biology
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Genome Biology
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Genomebiology.com
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Analysis
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Base Sequence
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Biotechnology & Applied Microbiology
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Chromosome Breakpoints
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Comparative Genomic Hybridization
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Dna
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Dna Copy Number Variations
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Dna Repair
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Genetic Aspects
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Genetics & Heredity
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Genome, Human
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Homologous Recombination
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Humans
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Introns
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Life Sciences & Biomedicine
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Messenger Rna
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Minisatellite Repeats
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Mutagenesis, Insertional
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Neurofibromatosis 1 - Genetics
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Neurofibromin 1 - Genetics
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