Auflistung nach Autor "Sauer, Alexandra"

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A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect

Kohl, Susanne; Sauer, Alexandra; Reuter, Peggy; Weisschuh, Nicole; Kempf, Melanie; Sliesoraityte, Ieva; Zrenner, Eberhart; Wissinger, Bernd; Llavona Juez, Pablo; Dehmelt, Florian A.; Arrenberg, Aristides; Kühlewein, Laura (2021)
Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1

Zobor, Ditta; Weckerle, Petra; Sauer, Alexandra; Wissinger, Bernd; Wilhelm, Helmut; Kohl, Susanne (2012)
Genes and Mutations in Autosomal Dominant Cone and Cone-Rod Dystrophy

Kohl, Susanne; Kitiratschky, Veronique; Papke, Monika; Schaich, Simone; Sauer, Alexandra; Wissinger, Bernd (2012)
Identification and characterization of a new locus associated with autosomal dominant cone dystrophy

Sauer, Alexandra (2015)

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