Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution.
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Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse modelsStructural variation mutagenesis of the human genome: Impact on disease and evolution.Fine-scale signatures of molecular evolution reconcile models of indel-associated mutationSimplification, Innateness, and the Absorption of Meaning from Context: How Novelty Arises from Gradual Network EvolutionGenome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.The effect of algorithms on copy number variant detection.Segmental duplication as one of the driving forces underlying the diversity of the human immunoglobulin heavy chain variable gene regionEvolution in health and medicine Sackler colloquium: Evolutionary perspectives on health and medicine.The characterisation of three types of genes that overlie copy number variable regionsThe association between DNA copy number aberrations at chromosome 5q22 and gastric cancerCopy number variation modifies expression time coursesOn the spot: very local chromosomal rearrangements.Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.Diversity in copy number and structure of a silkworm morphogenetic gene as a result of domestication.Structural variation-associated expression changes are paralleled by chromatin architecture modifications.FLNA genomic rearrangements cause periventricular nodular heterotopia.Mechanisms for recurrent and complex human genomic rearrangements.Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia.Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.Recent advances of genomic testing in perinatal medicineThe 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.Systematic Identification of Determinants for Single Strand Annealing Mediated Deletion Formation in Saccharomyces cerevisiaeThe molecular basis of α-thalassemia.Increased paternal age and the influence on burden of genomic copy number variation in the general population.The principles of teratology: are they still true?Analysis of the 9p21.3 sequence associated with coronary artery disease reveals a tendency for duplication in a CAD patient.Population-specific differences in gene conversion patterns between human SUZ12 and SUZ12P are indicative of the dynamic nature of interparalog gene conversion.Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH)
P2860
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P2860
Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Evolution in health and medici ...... man gene and genome evolution.
@ast
Evolution in health and medici ...... man gene and genome evolution.
@en
type
label
Evolution in health and medici ...... man gene and genome evolution.
@ast
Evolution in health and medici ...... man gene and genome evolution.
@en
prefLabel
Evolution in health and medici ...... man gene and genome evolution.
@ast
Evolution in health and medici ...... man gene and genome evolution.
@en
P2860
P356
P1476
Evolution in health and medici ...... man gene and genome evolution.
@en
P2093
Claudia M B Carvalho
James R Lupski
P2860
P304
P356
10.1073/PNAS.0906222107
P407
P478
107 Suppl 1
P50
P577
2010-01-13T00:00:00Z