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Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 79, doi. 10.1159/000184694
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- Article
Preface.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 5, doi. 10.1159/000184686
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CNVs and genetic medicine (excitement and consequences of a rediscovery).
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 7, doi. 10.1159/000184687
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Contents Vol. 123, 2008.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. I, doi. 10.1159/000209259
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- Article
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 65, doi. 10.1159/000184693
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Title Page / Table of Contents.
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- 2009
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- Table of Contents
Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 131, doi. 10.1159/000184700
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Detection and validation of copy number variation in X-linked mental retardation.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 44, doi. 10.1159/000184691
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- Article
CNV and nervous system diseases – what’s new?
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 54, doi. 10.1159/000184692
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Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 17, doi. 10.1159/000184688
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Copy variations in schizophrenia and bipolar disorder.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 27, doi. 10.1159/000184689
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- Article
The role of rare structural variants in the genetics of autism spectrum disorders.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 36, doi. 10.1159/000184690
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- Article
Benign and pathogenic copy number variation on the short arm of chromosome 4.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 88, doi. 10.1159/000184695
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- Article
Copy number variations in chronic pancreatitis.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 102, doi. 10.1159/000184697
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- Article
HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 156, doi. 10.1159/000184703
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- Article
Diseases associated with the low copy number of the C4B gene encoding C4, the fourth component of complement.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 118, doi. 10.1159/000184699
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- Article
Benign copy number changes in clinical cytogenetic diagnostics by array CGH.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 94, doi. 10.1159/000184696
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- Article
Copy number variants in genetic susceptibility and severity of systemic lupus erythematosus.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 142, doi. 10.1159/000184701
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- Article
The emerging role of structural variations in common disorders: initial findings and discovery challenges.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 108, doi. 10.1159/000184698
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- Article
Chromosome copy number variation and breast cancer risk.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 183, doi. 10.1159/000184707
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- Article
Copy number variation of Fc gamma receptor genes and disease predisposition.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 161, doi. 10.1159/000184704
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Copy number variation in metabolic phenotypes.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 169, doi. 10.1159/000184705
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- Article
Copy number alterations and copy number variation in cancer: close encounters of the bad kind.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 176, doi. 10.1159/000184706
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- Article
Copy number variation of beta-defensins and relevance to disease.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 148, doi. 10.1159/000184702
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- Article
Predisposition to colorectal cancer: exploiting copy number variation to identify novel predisposing genes and mechanisms.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 188, doi. 10.1159/000184708
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- Article
Copy number variation on the human Y chromosome.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 253, doi. 10.1159/000184715
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Sulfotransferase gene copy number variation: pharmacogenetics and function.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 205, doi. 10.1159/000184710
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Germline copy number variation in control populations.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 211, doi. 10.1159/000184711
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Large-scale copy number variants (CNVs) detected in different ethnic human populations.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 224, doi. 10.1159/000184712
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Human copy number polymorphic genes.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 234, doi. 10.1159/000184713
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CNVs of human genes and their implication in pharmacogenetics.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 195, doi. 10.1159/000184709
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Human subtelomeric copy number variations.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 244, doi. 10.1159/000184714
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Genomic drift and copy number variation of chemosensory receptor genes in humans and mice.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 263, doi. 10.1159/000184716
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Copy number variation and mosaicism.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 270, doi. 10.1159/000184717
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Expression divergence and copy number variation in the human genome.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 278, doi. 10.1159/000184718
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The evolutionary significance of copy number variation in the human genome.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 283, doi. 10.1159/000184719
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Comparative analysis of copy number variation in primate genomes.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 288, doi. 10.1159/000184720
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Computational methods for identification of recurrent copy number alteration patterns by array CGH.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 343, doi. 10.1159/000184726
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Author Index Vol. 123, 2008.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 352, doi. 10.1159/000209258
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- Article
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 322, doi. 10.1159/000184724
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Methods to detect and analyze copy number variations at the genome-wide and locus-specific levels.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 333, doi. 10.1159/000184725
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Copy number variation in the mouse genome: implications for the mouse as a model organism for human disease.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 297, doi. 10.1159/000184721
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CNV discovery using SNP genotyping arrays.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 307, doi. 10.1159/000184722
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Methods to detect CNVs in the human genome.
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- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 313, doi. 10.1159/000184723
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- Article