Zobrazeno 1 - 2
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pro vyhledávání: '"Julia Rundberg"'
Autor:
Irina Hüning, Lovisa Lovmar, Anna Erlandsson, Margarita Stefanova, Julia Rundberg, Kerstin Kutsche, Saideh Rajaei
Publikováno v:
European Journal of Medical Genetics. 56:188-191
The X-linked form of Opitz G/BBB syndrome is a congenital midline malformation syndrome caused by MID1 loss-of-function mutations, including point mutations and small-sized duplications, insertions, and deletions. Three patients with an Opitz G/BBB s
Autor:
Henry Ascher, Benedicte A. Lie, Julia Rundberg, Silja Svanstrøm Amundsen, Åsa Torinsson Naluai, Ludvig M. Sollid, A. H. Gudjonsdottir, Svetlana Adamovic, Johan Ek, Staffan Nilsson
Publikováno v:
Genes and immunity. 11(1)
Recent genome-wide association studies have identified 1q31 (RGS1), 2q11-12 (IL18RAP), 3p21 (CCR1/CCR3/CCR2), 3q25-26 (IL12A/SCHIP1), 3q28 (LPP), 4q27 (IL2/IL21), 6q25 (TAGAP) and 12q24 (SH2B3) as susceptibility regions for coeliac disease (CD). We h