Rezultati pretrage - Marija Guć‐Šćekić
- Prikaz rezultata 1 – 3 od 3
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1
Deletion and duplication screening in the DMD gene using MLPA od Tanja Lalic, Rolf H. A. M. Vossen, Jordy Coffa, Jan P. Schouten, Marija Guć‐Šćekić, Danijela Radivojevic, M Djurisić, Martÿn H. Breuning, Stefan J. White, Johan T. den Dunnen
Izdano 2005Artigo -
2
Complex small supernumerary marker chromosomes – an update od Thomas Liehr, Sanja Cirković, Tanja Lalic, Marija Guć‐Šćekić, Cynthia de Almeida, Jörg Weimer, Ivan Y. Iourov, Maria Melaragno, Roberta Santos Guilherme, Eunice‐Georgia G. Stefanou, Dilek Aktaş, Katharina Kreskowski, Elisabeth Klein, Monika Ziegler, Nadezda Kosyakova, Marianne Volleth, Ahmed B. Hamid
Izdano 2013Artigo -
3
Combined <scp>NGS</scp> Approaches Identify Mutations in the Intraflagellar Transport Gene <i>IFT140</i> in Skeletal Ciliopathies with Early Progressive Kidney Disease od Miriam Schmidts, Valeska Frank, Tobias Eisenberger, Saeed Al Turki, Albane A. Bizet, Dinu Antony, Suzanne Rix, Christian Decker, Nadine Bachmann, Martin Bald, Tobias Vinke, Burkhard Toenshoff, Nataliya Di Donato, Theresa Neuhann, Jane Hartley, Eamonn R. Maher, Radovan Bogdanović, Amira Peco‐Antić, Christoph J. Mache, Matthew E. Hurles, Ivana Joksić, Marija Guć‐Šćekić, Jelena Dobričić, Mirjana Branković-Magić, Hanno J. Bolz, Gregory J. Pazour, Philip L. Beales, Peter Scambler, Sophie Saunier, Hannah M. Mitchison, Carsten Bergmann
Izdano 2013Artigo
Alati za pretragu:
Povezani predmeti
Biology
Gene
Genetics
Anatomy
Bardet–Biedl syndrome
Bioinformatics
Breakpoint
Chromosomal translocation
Chromosome
Ciliogenesis
Ciliopathies
Ciliopathy
Cilium
Duchenne muscular dystrophy
Exon
Flagellum
Gene duplication
Intraflagellar transport
Joubert syndrome
Karyotype
Molecular biology
Multiplex
Multiplex ligation-dependent probe amplification
Multiplex polymerase chain reaction
Muscular dystrophy
Nephronophthisis
Penetrance
Phenotype
Polydactyly
Polymerase chain reaction