Incompletely Penetrant PKD1 Alleles Mimic the Renal Manifestations of ARPKD
VUJIC, Mihailo, HEYER, Christina M, BOGDANOVA, Nadja, HARRIS, Peter C, ARS, Elisabet, HOPP, Katharina, MARKOFF, Arseni, ÖRNDAL, Charlotte, RUDENHED, Bengt, NASR, Samih H, TORRES, Vicente E, TORRA, Roser
Published in Journal of the American Society of Nephrology (01.07.2010)
Published in Journal of the American Society of Nephrology (01.07.2010)
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Novel missense mutations in the glycine receptor β subunit gene ( GLRB ) in startle disease
James, Victoria M, Bode, Anna, Chung, Seo-Kyung, Gill, Jennifer L, Nielsen, Maartje, Cowan, Frances M, Vujic, Mihailo, Thomas, Rhys H, Rees, Mark I, Harvey, Kirsten, Keramidas, Angelo, Topf, Maya, Ginjaar, Ieke, Lynch, Joseph W, Harvey, Robert J
Published in Neurobiology of disease (01.04.2013)
Published in Neurobiology of disease (01.04.2013)
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Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea
Heinz-Erian, Peter, Müller, Thomas, Krabichler, Birgit, Schranz, Melanie, Becker, Christian, Rüschendorf, Franz, Nürnberg, Peter, Rossier, Bernard, Vujic, Mihailo, Booth, Ian W., Holmberg, Christer, Wijmenga, Cisca, Grigelioniene, Giedre, Kneepkens, C. M. Frank, Rosipal, Stefan, Mistrik, Martin, Kappler, Matthias, Michaud, Laurent, Dóczy, Ludwig-Christoph, Siu, Victoria Mok, Krantz, Marie, Zoller, Heinz, Utermann, Gerd, Janecke, Andreas R.
Published in American journal of human genetics (13.02.2009)
Published in American journal of human genetics (13.02.2009)
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Identification of the gene responsible for Best macular dystrophy
Petrukhin, Konstantin, Wadelius, Claes, Koisti, Markus J, Bakall, Benjamin, Li, Wen, Xie, Guochun, Marknell, Towa, Sandgren, Ola, Forsman, Kristina, Holmgren, Gösta, Andreasson, Sten, Vujic, Mihailo, Bergen, Arthur A. B, McGarty-Dugan, Valarie, Figueroa, David, Austin, Christopher P, Metzker, Michael L, Caskey, C.Thomas
Published in Nature genetics (01.07.1998)
Published in Nature genetics (01.07.1998)
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Functional analysis of the novel TBX5 c.1333delC mutation resulting in an extended TBX5 protein
Böhm, Johann, Heinritz, Wolfram, Craig, Alexander, Vujic, Mihailo, Ekman-Joelsson, Britt-Marie, Kohlhase, Jürgen, Froster, Ursula
Published in BMC medical genetics (01.10.2008)
Published in BMC medical genetics (01.10.2008)
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A new greenhouse invader: the first report of the alien ring-legged earwig, Euborellia annulipes (Dermaptera, Anisolabididae) in Serbia, with the first checklist of earwigs of the country
Vujić, Mihailo, Vesović, Nikola, Šević, Mirko, Maričić, Marko, Tot, Ivan
Published in Travaux du Muséum national d'histoire naturelle "Grigore Antipa" (2022)
Published in Travaux du Muséum national d'histoire naturelle "Grigore Antipa" (2022)
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A case report of two male siblings with autism and duplication of Xq13–q21, a region including three genes predisposing for autism
Wentz, Elisabet, Vujic, Mihailo, Kärrstedt, Ewa-Lotta, Erlandsson, Anna, Gillberg, Christopher
Published in European child & adolescent psychiatry (01.05.2014)
Published in European child & adolescent psychiatry (01.05.2014)
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Functional analysis of the novel TBX5 c. 1333delC mutation resulting in an extended TBX5 protein
Boehm, Johann, Heinritz, Wolfram, Craig, Alexander, Vujic, Mihailo, Ekman-Joelsson, Britt-Marie, Kohlhase, Juergen, Froster, Ursula
Published in BMC medical genetics (01.10.2008)
Published in BMC medical genetics (01.10.2008)
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First record of the genus Xeropicta Monterosato, 1892 (Gastropoda: Eupulmonata: Geomitridae) in Serbia
Gojšina, Vukašin, Páll-Gergely, Barna, Vujić, Mihailo, Dedov, Ivailo
Published in Folia malacologica (01.03.2022)
Published in Folia malacologica (01.03.2022)
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Functional analysis of the novel TBX5c.1333delC mutation resulting in an extended TBX5 protein
Böhm, Johann, Heinritz, Wolfram, Craig, Alexander, Vujic, Mihailo, Ekman-Joelsson, Britt-Marie, Kohlhase, Jürgen, Froster, Ursula
Published in BMC medical genetics (01.10.2008)
Published in BMC medical genetics (01.10.2008)
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Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes
Vujic, Mihailo, Bergman, Annika, Romanus, Bertil, Wahlström, Jan, Martinsson, Tommy
Published in International journal of molecular medicine (01.01.2004)
Published in International journal of molecular medicine (01.01.2004)
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Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization
Blennow, E, Bui, T H, Kristoffersson, U, Vujic, M, Annerén, G, Holmberg, E, Nordenskjöld, M
Published in Prenatal diagnosis (01.11.1994)
Published in Prenatal diagnosis (01.11.1994)
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