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Zofia Kijas

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Wei Chen; Vera Kalscheuer; Andreas Tzschach; Corinna Menzel; Reinhard Ullmann; Marcel Holger Schulz; Fikret Erdogan; Na Li; Zofia Kijas; Ger Arkesteijn; Isidora Lopez Pajares; Margret Goetz-Sothmann; Uwe Heinrich; Imma Rost; Andreas Dufke; Ute Grasshoff; Birgitta Glaeser; Martin Vingron; Hans-Hilger Ropers
Mapping translocation breakpoints by next-generation sequencing.
Joyce So; Vanessa Suckow; Zofia Kijas; Vera Kalscheuer; Bettina Moser; Jennifer Winter; Marieke Baars; Helen V Firth; Peter Lunt; Ben Hamel; Peter Meinecke; Claude Moraine; Sylvie Odent; Albert Schinzel; Jasper van der Smagt; koenraad devriendt; Beate Albrecht; Gabriele Gillessen-Kaesbach; Ineke van der Burgt; Fred Petrij; Laurence Faivre; Julie McGaughran; Fiona McKenzie; John M Opitz; Timothy Cox; Susann Schweiger
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.
Jennifer Winter; Tanja Lehmann; Sybille Krauss; Alexander Trockenbacher; Zofia Kijas; John Foerster; Vanessa Suckow; Marie-Laure Yaspo; Andreas E Kulozik; Vera Kalscheuer; Rainer Schneider; Susann Schweiger
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing.

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All Publications

2008: Wei Chen; Vera Kalscheuer; Andreas Tzschach; Corinna Menzel; Reinhard Ullmann; Marcel Holger Schulz; Fikret Erdogan; Na Li; Zofia Kijas; Ger Arkesteijn; Isidora Lopez Pajares; Margret Goetz-Sothmann; Uwe Heinrich; Imma Rost; Andreas Dufke; Ute Grasshoff; Birgitta Glaeser; Martin Vingron; Hans-Hilger Ropers
Mapping translocation breakpoints by next-generation sequencing.
Genome research 2008;18(7):1143-9.
2005: Joyce So; Vanessa Suckow; Zofia Kijas; Vera Kalscheuer; Bettina Moser; Jennifer Winter; Marieke Baars; Helen V Firth; Peter Lunt; Ben Hamel; Peter Meinecke; Claude Moraine; Sylvie Odent; Albert Schinzel; Jasper van der Smagt; koenraad devriendt; Beate Albrecht; Gabriele Gillessen-Kaesbach; Ineke van der Burgt; Fred Petrij; Laurence Faivre; Julie McGaughran; Fiona McKenzie; John M Opitz; Timothy Cox; Susann Schweiger
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.
American journal of medical genetics. Part A 2005;132A(1):1-7.
2004: Jennifer Winter; Tanja Lehmann; Sybille Krauss; Alexander Trockenbacher; Zofia Kijas; John Foerster; Vanessa Suckow; Marie-Laure Yaspo; Andreas E Kulozik; Vera Kalscheuer; Rainer Schneider; Susann Schweiger
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing.
Human genetics 2004;114(6):541-52.
2004: John Foerster; Ilja Nolte; Susann Schweiger; Claudia Ehlert; Marcel Bruinenberg; Katja Spaar; Gerrit van der Steege; Marcel Mulder; Vera Kalscheuer; Bettina Moser; Zofia Kijas; Petra Seeman; Markward Ständer; Wolfram Sterry; Gerard te Meerman
Evaluation of the IRF-2 gene as a candidate for PSORS3.
The Journal of investigative dermatology 2004;122(1):61-4.
2003: Jennifer Winter; Tanja Lehmann; Vanessa Suckow; Zofia Kijas; Andreas E Kulozik; Vera Kalscheuer; Ben Hamel; koenraad devriendt; John M Opitz; Steffen Lenzner; Hans-Hilger Ropers; Susann Schweiger
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome.
Human genetics 2003;112(3):249-54.