Search Results - Maria Wilbe

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  1. 1

    Equine multiple congenital ocular anomalies and silver coat colour result from the pleiotropic effects of mutant PMEL. by Lisa S Andersson, Maria Wilbe, Agnese Viluma, Gus Cothran, Björn Ekesten, Susan Ewart, Gabriella Lindgren

    Published in PLoS ONE (2013-01-01)
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  2. 2

    A novel quantitative targeted analysis of X-chromosome inactivation (XCI) using nanopore sequencing by Josefin Johansson, Sarah Lidéus, Ida Höijer, Adam Ameur, Sanna Gudmundsson, Göran Annerén, Marie-Louise Bondeson, Maria Wilbe

    Published in Scientific Reports (2023-08-01)
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  3. 3

    Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen... by K. Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson, Eva-Lena Stattin, Ruma Raha-Chowdhury, Roger Williams

    Published in Hereditas (2017-12-01)
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  4. 4

    Correction: DLA Class II Alleles Are Associated with Risk for Canine Symmetrical Lupoid Onychodystrophy (SLO). by Maria Wilbe, Martine Lund Ziener, Anita Aronsson, Charlotte Harlos, Katarina Sundberg, Elin Norberg, Lisa Andersson, Kerstin Lindblad-Toh, Åke Hedhammar, Göran Andersson, Frode Lingaas

    Published in PLoS ONE (2010-01-01)
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  5. 5

    DLA class II alleles are associated with risk for canine symmetrical lupoid onychodystrophy [corrected](SLO). by Maria Wilbe, Martine Lund Ziener, Anita Aronsson, Charlotte Harlos, Katarina Sundberg, Elin Norberg, Lisa Andersson, Kerstin Lindblad-Toh, Ake Hedhammar, Göran Andersson, Frode Lingaas

    Published in PLoS ONE (2010-01-01)
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