about
A high-resolution map of synteny disruptions in gibbon and human genomesTiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumorsAlgebraic correction methods for computational assessment of clone overlaps in DNA fingerprint mappingComplex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndromeCGHPRO -- a comprehensive data analysis tool for array CGH.Minimal cross-recombination between wild-type and loxP511 sites in vivo facilitates truncating both ends of large DNA inserts in pBACe3.6 and related vectors.Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patientsGenome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysisEvolutionary breakpoints in the gibbon suggest association between cytosine methylation and karyotype evolutionCommon variants at 19p13 are associated with susceptibility to ovarian cancer.Duplication 8q12: confirmation of a novel recognizable phenotype with duane retraction syndrome and developmental delayTraffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome.A sequence-based survey of the complex structural organization of tumor genomes.High-resolution array CGH clarifies events occurring on 8p in carcinogenesisA multiway analysis for identifying high integrity bovine BACs.Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias of the breast.Diagnostic genome profiling in mental retardation.Identification by full-coverage array CGH of human DNA copy number increases relative to chimpanzee and gorilla.Decoding the fine-scale structure of a breast cancer genome and transcriptome.Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.The new cytogenetics: blurring the boundaries with molecular biology.A comprehensive molecular cytogenetic analysis of chromosome rearrangements in gibbons.A BAC clone fingerprinting approach to the detection of human genome rearrangementsDiagnostic genome profiling: unbiased whole genome or targeted analysis?Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes.Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.From cytogenetics to next-generation sequencing technologies: advances in the detection of genome rearrangements in tumors.Identifying Distal cis-acting Gene-Regulatory Sequences by Expressing BACs Functionalized with loxP-Tn10 Transposons in Zebrafish.Analysis of molecular cytogenetic alterations in uterine leiomyosarcoma by array-based comparative genomic hybridization.Genome position and gene amplificationThe lymphovascular embolus of inflammatory breast cancer exhibits a Notch 3 addiction.Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.Chromosome 5p aberrations are early events in lung cancer: implication of glial cell line-derived neurotrophic factor in disease progression.Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
A set of BAC clones spanning the human genome.
@en
type
label
A set of BAC clones spanning the human genome.
@en
prefLabel
A set of BAC clones spanning the human genome.
@en
P2093
P2860
P356
P1476
A set of BAC clones spanning the human genome.
@en
P2093
Alison Cloutier
Amara Masson
Anna-Liisa Prabhu
Carrie Mathewson
Chik-On Choy
Darlene Lee
Donna Albertson
Duane Smailus
Eric Schoenmakers
Ian Bosdet
P2860
P304
P356
10.1093/NAR/GKH700
P407
P50
P577
2004-07-09T00:00:00Z