Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
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High prevalence of SLC6A8 deficiency in X-linked mental retardationShwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersAnalysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromereCreatine synthesis and transport during rat embryogenesis: spatiotemporal expression of AGAT, GAMT and CT1.Retroviruses and primate evolutionA genome-wide comparison of recent chimpanzee and human segmental duplicationsGenome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmiasThe mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genomeEvolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoidsChance favors the prepared genome.Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome.Mapping segmental and sequence variations among laboratory mice using BAC array CGH.Molecular approaches to the Rett syndrome gene.Punctuated duplication seeding events during the evolution of human chromosome 2p11.An Alu transposition model for the origin and expansion of human segmental duplications.Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEMasquerading repeats: paralogous pitfalls of the human genome.Evidence for widespread reticulate evolution within human dupliconsCircular DNA intermediate in the duplication of Nile tilapia vasa genes.A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes.Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.Pericentromeric duplications in the laboratory mouse.Efficient approach to unique single-nucleotide polymorphism discovery.Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21.Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15qDirectly transmitted unbalanced chromosome abnormalities and euchromatic variants16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.The creatine transporter gene paralogous at 16p11.2 is expressed in human brain.Recent segmental duplications in the working draft assembly of the brown Norway rat.X-linked creatine transporter deficiency: clinical aspects and pathophysiology.Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions.Segmental duplications: organization and impact within the current human genome project assembly.Retrotransposon-related DNA sequences in the centromeres of grass chromosomes.Cloning and characterization of a novel mouse Siglec, mSiglec-F: differential evolution of the mouse and human (CD33) Siglec-3-related gene clusters.New creatine transporter assay and identification of distinct creatine transporter isoforms in muscle.
P2860
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P2860
Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@en
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@nl
type
label
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@en
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@nl
prefLabel
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@en
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@nl
P2093
P356
P1476
Duplication of a gene-rich clu ...... r paralogous genome evolution.
@en
P2093
Doggett NA
Eichler EE
P304
P356
10.1093/HMG/5.7.899
P577
1996-07-01T00:00:00Z