Pages that link to "Q34439696"
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The following pages link to Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH. (Q34439696):
Displayed 50 items.
- The diploid genome sequence of an individual human (Q21090194) (← links)
- High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays (Q24545276) (← links)
- Clinical and molecular delineation of the 17q21.31 microdeletion syndrome (Q24624737) (← links)
- Paired-end mapping reveals extensive structural variation in the human genome (Q24653260) (← links)
- GDF6, a novel locus for a spectrum of ocular developmental anomalies (Q24680270) (← links)
- Comparative isoschizomer profiling of cytosine methylation: the HELP assay (Q24685607) (← links)
- BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH) (Q25257750) (← links)
- A high-resolution map of segmental DNA copy number variation in the mouse genome (Q27315085) (← links)
- An optimized microarray platform for assaying genomic variation in Plasmodium falciparum field populations (Q28031409) (← links)
- Fancf-deficient mice are prone to develop ovarian tumours (Q28247935) (← links)
- Chromosome Conformation Capture Carbon Copy (5C): a massively parallel solution for mapping interactions between genomic elements (Q28262061) (← links)
- Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis (Q28293141) (← links)
- Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes (Q28306123) (← links)
- Loss of p53 partially rescues embryonic development of Palb2 knockout mice but does not foster haploinsufficiency of Palb2 in tumour suppression (Q28512158) (← links)
- Chromosome 12p deletions in TEL-AML1 childhood acute lymphoblastic leukemia are associated with retrotransposon elements and occur postnatally (Q28756307) (← links)
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Q29614573) (← links)
- Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells (Q29619469) (← links)
- Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy (Q30489316) (← links)
- Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5. (Q30528737) (← links)
- Maize inbreds exhibit high levels of copy number variation (CNV) and presence/absence variation (PAV) in genome content (Q30940430) (← links)
- Global MYCN transcription factor binding analysis in neuroblastoma reveals association with distinct E-box motifs and regions of DNA hypermethylation (Q30974276) (← links)
- Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors (Q31030415) (← links)
- Identification of candidate genes involved in neuroblastoma progression by combining genomic and expression microarrays with survival data. (Q31113973) (← links)
- wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data (Q31149372) (← links)
- Resolving the resolution of array CGH. (Q33271882) (← links)
- Oligonucleotide Array Comparative Genomic Hybridization (oaCGH) based characterization of genetic deficiencies as an aid to gene mapping in Caenorhabditis elegans (Q33305159) (← links)
- An integrative genomic and epigenomic approach for the study of transcriptional regulation (Q33325492) (← links)
- A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the human NBPF1 and ACCN1 genes (Q33336547) (← links)
- High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene (Q33355806) (← links)
- A snapshot of CNVs in the pig genome (Q33392713) (← links)
- Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis (Q33412120) (← links)
- Chromatin conformation signatures of cellular differentiation (Q33431476) (← links)
- Comparative genomic hybridization: microarray design and data interpretation (Q33432993) (← links)
- Integrating sequencing technologies in personal genomics: optimal low cost reconstruction of structural variants (Q33480954) (← links)
- Widespread dysregulation of MiRNAs by MYCN amplification and chromosomal imbalances in neuroblastoma: association of miRNA expression with survival (Q33516231) (← links)
- Recurrent genomic imbalances in primary effusion lymphomas (Q33562285) (← links)
- Copy number variation in the bovine genome (Q33574937) (← links)
- Distinct high resolution genome profiles of early onset and late onset colorectal cancer integrated with gene expression data identify candidate susceptibility loci (Q33575005) (← links)
- Transcriptomics technologies. (Q33703532) (← links)
- High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset (Q33732709) (← links)
- Genome-wide polymorphisms and development of a microarray platform to detect genetic variations in Plasmodium yoelii (Q33737114) (← links)
- Novel origins of copy number variation in the dog genome (Q33741770) (← links)
- A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay (Q33763087) (← links)
- Analysis of copy number variations among diverse cattle breeds. (Q33812603) (← links)
- Detection of copy number variations and their effects in Chinese bulls (Q33815116) (← links)
- High-throughput 454 resequencing for allele discovery and recombination mapping in Plasmodium falciparum (Q33821609) (← links)
- Chromosomal and microRNA expression patterns reveal biologically distinct subgroups of 11q- neuroblastoma (Q33891984) (← links)
- Promoter hypermethylation in MLL-r infant acute lymphoblastic leukemia: biology and therapeutic targeting. (Q33931890) (← links)
- Detection of copy number variations in rice using array-based comparative genomic hybridization (Q33965586) (← links)
- Identification of genomic indels and structural variations using split reads (Q33970542) (← links)