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.
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Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional geneUrinary tract effects of HPSE2 mutations.Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux.Genetic, environmental, and epigenetic factors involved in CAKUT.Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract.Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.
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P2860
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.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 07 July 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A new genome scan for primary ...... in urinary tract development.
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A new genome scan for primary ...... in urinary tract development.
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type
label
A new genome scan for primary ...... in urinary tract development.
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A new genome scan for primary ...... in urinary tract development.
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prefLabel
A new genome scan for primary ...... in urinary tract development.
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A new genome scan for primary ...... in urinary tract development.
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A new genome scan for primary ...... d in urinary tract development
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C M Molony
H J Cordell
J M Darlow
M G Dobson
M Hunziker
P2860
P356
10.1002/MGG3.22
P577
2013-07-07T00:00:00Z