Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations

scientific article published on 8 December 2007

Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/NDT/GFM685
P698PubMed publication ID18065799
P5875ResearchGate publication ID5782136

P50authorElijah O KehindeQ117856085
P2093author name stringBethan E Hoskins
Friedhelm Hildebrandt
Shazia Ashraf
Velibor Tasic
Carl H Cramer
Radovan Bogdanovic
Julia Hoefele
Martin Pohl
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)777-779
P577publication date2007-12-08
P1433published inNephrology Dialysis TransplantationQ15710302
P1476titleMissense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations
P478volume23

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cites work (P2860)
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Q33692509Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract
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Q38217616The HNF1B score is a simple tool to select patients for HNF1B gene analysis
Q90712113The copy number variation landscape of congenital anomalies of the kidney and urinary tract

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