Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics
about
Chromosomes in the flow to simplify genome analysisHuman molecular cytogenetics: From cells to nucleotidesCharacterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing dataExplorations to improve the completeness of exome sequencingA chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report.Detection of chromosomal breakpoints in patients with developmental delay and speech disordersChromosomal polymorphism in two species of Hypancistrus (Siluriformes: Loricariidae): an integrative approach for understanding their biodiversity.Comprehensive Analysis of Genome Rearrangements in Eight Human Malignant Tumor TissuesAccurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing.Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing.Germline copy number variations and cancer predisposition.Copy number variation in the cattle genome.The role of high-throughput technologies in clinical cancer genomics.Non-invasive prenatal testing for aneuploidy: current status and future prospects.The molecular landscape of pediatric brain tumors in the next-generation sequencing era.Concise review: Genomic instability in human stem cells: current status and future challenges.The current state of molecular cytogenetics in cancer diagnosis.Whole-genome CNV analysis: advances in computational approachesGenomic Instability of iPSCs: Challenges Towards Their Clinical Applications.Evolution of genetic techniques: past, present, and beyond.Identification of minor chromosomal defects causing abnormal foetus and spontaneous abortions.Molecular cytogenetics: karyotype evolution, phylogenomics and future prospects.Cytogenomics of Feline Cancers: Advances and Opportunities.Partial duplication of chromosome 19 associated with syndromic duane retraction syndrome.Long-read genome sequencing identifies causal structural variation in a Mendelian disease.Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.CCDD Phenotype Associated with a Small Chromosome 2 Deletion.Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome.The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.Full Karyotype Interphase Cell Analysis.
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P2860
Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
Characterising chromosome rear ...... nces in molecular cytogenetics
@en
Characterising chromosome rear ...... ces in molecular cytogenetics.
@nl
type
label
Characterising chromosome rear ...... nces in molecular cytogenetics
@en
Characterising chromosome rear ...... ces in molecular cytogenetics.
@nl
prefLabel
Characterising chromosome rear ...... nces in molecular cytogenetics
@en
Characterising chromosome rear ...... ces in molecular cytogenetics.
@nl
P2860
P356
P1433
P1476
Characterising chromosome rear ...... nces in molecular cytogenetics
@en
P2093
S Le Scouarnec
S M Gribble
P2860
P2888
P356
10.1038/HDY.2011.100
P407
P577
2011-11-16T00:00:00Z
2012-01-01T00:00:00Z