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scopus: 36436931000

Husen, M.

(Margreet Husen)


vacterl association polyalanine atresia patient mutation association vacterl zic 3 tracheo-oesophageal fi stula genet x-linked heterotaxy heterotaxy zic 3 gene expansion heart stula situs x-linked oesophageal atresia syndrome defect zic 3 mutations oesophageal anomaly anal atresia vena cava kidney zic 3 mutation stenosi protein tracheo-oesophageal disease feature esophageal atresia group.bmj.com letter tracheoesophageal fi stula department 6- nucleotide insertion right alanine abnormality transcription casey b netherland table polyalanine stretch malformations factor polyalanine expansion mother deletion novel erasmu stretch dextroposition esophageal asplenia rotterdam malformation center tract transcription factor zic 3 polyalanine chromosome outlet right ventricle ambiguu polyalanine expansion diseases casey stomach jmg.bmj.com inversu identi fied polyalanine expansions article downloaded polyalanine domains speci fied insertion multicystic kidney muenke m




1 Most Recent Publications

Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: A new polyalanine disorder? (Article)
Wessels, M.W. Kuchina, B. Casey, B. Heydanus, R. Smit, B.J. Dooijes, D. Krijger, R.R. de Lequin, M.H. Jong, E.M. de Husen, M. Willems, P.J.
2010-05-01