about
Patterns of Chromosomal Aberrations in Solid TumorsMolecular diagnosis of chronic granulomatous diseaseCongenital myasthenic syndromes: pathogenesis, diagnosis, and treatmentClinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal casesNetwork-based drug discovery by integrating systems biology and computational technologiesRecurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head sizeGenome-wide copy number analysis of single cells.Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastomaCGHpower: exploring sample size calculations for chromosomal copy number experiments.Isolation of disseminated neuroblastoma cells from bone marrow aspirates for pretreatment risk assessment by array comparative genomic hybridization.Integrated analysis of gene expression and copy number data on gene shaving using independent component analysisIdentification of clinically important chromosomal aberrations in acute myeloid leukemia by array-based comparative genomic hybridization.Genomic profile of copy number variants on the short arm of human chromosome 8.Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH.Molecular karyotyping of human single sperm by array- comparative genomic hybridizationCopy number variants in locally raised Chinese chicken genomes determined using array comparative genomic hybridizationCopy number variants in pharmacogenetic genes.Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?Current status of the congenital myasthenic syndromes.Clinical Trial of Human Fetal Brain-Derived Neural Stem/Progenitor Cell Transplantation in Patients with Traumatic Cervical Spinal Cord Injury.A discovery resource of rare copy number variations in individuals with autism spectrum disorder.MICrocephaly, disproportionate pontine and cerebellar hypoplasia syndrome: A clinico-radiologic phenotype linked to calcium/calmodulin-dependent serine protein kinase gene mutation.Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines.New tools for functional genomic analysis.Integration of cancer genomics with treatment selection: from the genome to predictive biomarkersDeciphering genetic disease in the genomic era: the model of GnRH deficiency.Clinical, pathological and molecular determinants in squamous cell carcinoma of the oral cavity.Smith-Magenis syndrome: haploinsufficiency of RAI1 results in altered gene regulation in neurological and metabolic pathways.Genetic testing in renal disease.Cancer proteomics.Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.Developmental psychopathology: the role of structural variation in the genome.Disorders of sex development: effect of molecular diagnostics.Advances in the role of cytogenetic analysis in the molecular diagnosis of B-cell lymphomas.The cost of molecular-guided therapy in oncology: a prospective cost study alongside the MOSCATO trial.Integrated analysis of whole genome exon array and array-comparative genomic hybridization in gastric and colorectal cancer cells.Expanding probe repertoire and improving reproducibility in human genomic hybridization.Immortalization of epithelial cells in oral carcinogenesis as revealed by genome-wide array comparative genomic hybridization: A meta-analysis.Application of microarray-based comparative genomic hybridization in prenatal and postnatal settings: three case reports.14q32 deletion syndrome: a clinical report.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
The array CGH and its clinical applications.
@ast
The array CGH and its clinical applications.
@en
The array CGH and its clinical applications.
@nl
type
label
The array CGH and its clinical applications.
@ast
The array CGH and its clinical applications.
@en
The array CGH and its clinical applications.
@nl
prefLabel
The array CGH and its clinical applications.
@ast
The array CGH and its clinical applications.
@en
The array CGH and its clinical applications.
@nl
P1433
P1476
The array CGH and its clinical applications.
@en
P2093
Marwan Shinawi
Sau Wai Cheung
P304
P356
10.1016/J.DRUDIS.2008.06.007
P577
2008-07-17T00:00:00Z