A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation von Rodriguez-Polo, Ignacio, Mißbach, Sophie, Petkov, Stoyan, Mattern, Felix, Maierhofer, Anna, Grządzielewska, Iga, Tereshchenko, Yuliia, Urrutia-Cabrera, Daniel, Haaf, Thomas, Dressel, Ralf, Bartels, Iris, Behr, Rüdiger

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Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22 von Schnabel, Franziska, Smogavec, Mateja, Funke, Rudolf, Pauli, Silke, Burfeind, Peter, Bartels, Iris

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Non-Human Primate iPSC Generation, Cultivation, and Cardiac Differentiation under Chemically Defined Conditions von Stauske, Michael, Polo, Ignacio Rodriguez, Haas, Wadim, Knorr, Debbra Yasemin, Borchert, Thomas, Streckfuss-Boemeke, Katrin, Dressel, Ralf, Bartels, Iris, Tiburcy, Malte, Zimmermann, Wolfram-Hubertus, Behr, Ruediger

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Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification von Starke, Heike, Nietzel, Angela, Weise, Anja, Heller, Anita, Mrasek, Kristin, Belitz, Britta, Kelbova, Christine, Volleth, Marianne, Albrecht, Beate, Mitulla, Beate, Trappe, Ralf, Bartels, Iris, Adolph, Sabine, Dufke, Andreas, Singer, Sylke, Stumm, Markus, Wegner, Rolf-Dieter, Seidel, Jörg, Schmidt, Angela, Kuechler, Alma, Schreyer, Isolde, Claussen, Uwe, von Eggeling, Ferdinand, Liehr, Thomas

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Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation von Auber, Bernd, Bruemmer, Verena, Zoll, Barbara, Burfeind, Peter, Boehm, Detlef, Liehr, Thomas, Brockmann, Knut, Wilichowski, Ekkehard, Argyriou, Loukas, Bartels, Iris

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Cell-free fetal DNA in specimen from pregnant women is stable up to 5days von Anon., Anon

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Baboon induced pluripotent stem cell generation by piggyBac transposition of reprogramming factors von Rodriguez-Polo, Ignacio, Stauske, Michael, Becker, Alexander, Bartels, Iris, Dressel, Ralf, Behr, Rüdiger

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The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible von Müller, Sina P., Bartels, Iris, Stein, Werner, Emons, Günther, Gutensohn, Kai, Köhler, Michael, Legler, Tobias J.

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Baboon induced pluripotent stem cell generation by piggyBac transposition of reprogramming factors von Rodriguez-Polo, Ignacio, Stauske, Michael, Becker, Alexander, Bartels, Iris, Dressel, Ralf, Behr, Rüdiger

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Cell-free fetal DNA in specimen from pregnant women is stable up to 5 days von Müller, Sina P., Bartels, Iris, Stein, Werner, Emons, Günter, Gutensohn, Kai, Legler, Tobias J.

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Suicide Inactivation of Catechol 2,3-Dioxygenase from Pseudomonas putida mt-2 by 3-Halocatechols von BARTELS, I, KNACKMUSS, H.-J, REINEKE, W

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Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes von Pauli, Silke, Schmidt, Thomas, Funke, Rudolf, Zoll, Barbara, Burfeind, Peter, Dybowski, Ursula, Shoukier, Moneef, Bartels, Iris

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Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p von Bartels, Iris, Pütz, Irene, Reintjes, Nadine, Netzer, Christian, Shoukier, Moneef

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De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis von Schwaibold, Eva Maria Christina, Bartels, Iris, Küster, Helmut, Lorenz, Michael, Burfeind, Peter, Adam, Ronja, Zoll, Barbara

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A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect von Shoukier, Moneef, Wickert, Julia, Schröder, Julia, Bartels, Iris, Auber, Bernd, Zoll, Barbara, Salinas‐Riester, Gabriela, Weise, Dagmar, Brockmann, Knut, Zirn, Birgit, Burfeind, Peter

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An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype von Bartels, Iris, Starke, Heike, Argyriou, Loukas, Sauter, Simone M, Zoll, Barbara, Liehr, Thomas

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Biochemical screening for chromosomal disorders and neural tube defects (NTD): is adjustment of maternal alpha-fetoprotein (AFP) still appropriate in insulin-dependent diabetes mel... von Sancken, Ulrich, Bartels, Iris

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Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage von EIBEN, B, BARTELS, I, RAUSKOLB, R, HANSMANN, I, BAÊHR-PORSCH, S, BORGMANN, S, GATZ, G, GELLERT, G, GOEBEL, R, HAMMANS, W, HENTEMANN, M, OSMERS, R

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Partial trisomy of distal 19q detected by quantitative real‐time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay von Sauter, S.M., Böhm, Detlef, Bartels, Iris, Burfeind, Peter, Laccone, Franco A., Neesen, Jürgen, Wilken, Bernd, Liehr, Thomas, Zoll, Barbara

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Prenatal detection of X-linked ichthyosis by maternal serum screening for down syndrome von Bartels, Iris, Caesar, Julius, Sancken, Ulrich

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