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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3. Hum Mol Genet. 2015 Jul 15; 24(14):4061-77.
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PubMed
subject areas
Alleles
Alu Elements
Base Sequence
Chromosomes, Human, Pair 17
Comparative Genomic Hybridization
DNA Copy Number Variations
Female
Gene Duplication
Gene Rearrangement
Genome, Human
Genomic Instability
Genomics
Homologous Recombination
Humans
Male
Molecular Sequence Data
Segmental Duplications, Genomic
Sequence Deletion
authors with profiles
PAWEL STANKIEWICZ
CHAD SHAW
SAU WAI CHEUNG
CARLOS BACINO
JAMES LUPSKI
SANDESH NAGAMANI