Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.
about
Evolutionary history and genome organization of DUF1220 protein domainsSingle-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humansGenetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigeneticsProximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesCopy-number variation analysis in familial nonsyndromic congenital anomalies of the kidney and urinary tract: Evidence for the causative role of a transposable element-associated genomic rearrangement.Exploring the genetic basis of early-onset chronic kidney disease.Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome.Genetic Basis of Ureterocele.Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions.Genes, Exomes, Genomes, Copy Number: What is Their Future in Pediatric Renal Disease.1q21.1 Microduplication expression in adults.A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development.Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract.Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.Genomic medicine for kidney disease.Unusual association between cardiac, skeletal, urogenital and renal abnormalities.Copy-number variation associated with congenital anomalies of the kidney and urinary tract.De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome.
P2860
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P2860
Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.
description
2010 nî lūn-bûn
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2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
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name
Mapping candidate regions and ...... arative genomic hybridization.
@en
Mapping candidate regions and ...... the kidneys and urinary tract
@nl
type
label
Mapping candidate regions and ...... arative genomic hybridization.
@en
Mapping candidate regions and ...... the kidneys and urinary tract
@nl
prefLabel
Mapping candidate regions and ...... arative genomic hybridization.
@en
Mapping candidate regions and ...... the kidneys and urinary tract
@nl
P2093
P2860
P356
P1476
Mapping candidate regions and ...... arative genomic hybridization.
@en
P2093
Christina Landwehr
Dieter Haffner
Franz Schaefer
Jonas Denecke
Miriam Renkert
Ruthild G Weber
Stefanie Weber
P2860
P304
P356
10.1093/NDT/GFQ400
P407
P577
2010-07-05T00:00:00Z