Hasil Pencarian - Maria Wilbe

  • Menampilkan 1 - 7 hasil dari 7
Perbaiki Hasil
  1. 1
    Equine multiple congenital ocular anomalies and silver coat colour result from the pleiotropic effects of mutant PMEL.

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

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    A novel quantitative targeted analysis of X-chromosome inactivation (XCI) using nanopore sequencing

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

    Diterbitkan 2023-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  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 genes

    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... oleh K. Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson, Eva-Lena Stattin, Ruma Raha-Chowdhury, Roger Williams

    Diterbitkan 2017-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Correction: DLA Class II Alleles Are Associated with Risk for Canine Symmetrical Lupoid Onychodystrophy (SLO).

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

    Diterbitkan 2010-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    DLA class II alleles are associated with risk for canine symmetrical lupoid onychodystrophy [corrected](SLO).

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

    Diterbitkan 2010-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

    Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity oleh Ida Höijer, Josefin Johansson, Sanna Gudmundsson, Chen-Shan Chin, Ignas Bunikis, Susana Häggqvist, Anastasia Emmanouilidou, Maria Wilbe, Marcel den Hoed, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur

    Diterbitkan 2020-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease.

    Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease. oleh Maria Wilbe, Sergey V Kozyrev, Fabiana H G Farias, Hanna D Bremer, Anna Hedlund, Gerli R Pielberg, Eija H Seppälä, Ulla Gustafson, Hannes Lohi, Örjan Carlborg, Göran Andersson, Helene Hansson-Hamlin, Kerstin Lindblad-Toh

    Diterbitkan 2015-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: