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  1. Heine, Marcella [Editor]

    Wir sind Kinder einer Welt - [1. Aufl.]

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    Stuttgart; Düsseldorf; Berlin; Leipzig: Klett-Schulbuchverl., 1994

    Published in: Lesehefte Welt- und Umweltkunde ; Neue Folge

  3. Al-Oweini, Rami [Author] ; Kortz, Ulrich [Degree supervisor]; Röschenthaler, Gerd-Volker [Degree supervisor]; Bonchio, Marcella [Degree supervisor]; Heine, Thomas [Degree supervisor]; Bassil, Bassem [Degree supervisor]

    Synthesis and Characterization of Multinuclear Manganese-Containing Polyoxotungstates for Homogeneous Water-Oxidation Catalysis

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    Bremen: IRC-Library, Information Resource Center der Jacobs University Bremen, 2013

  4. Mlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; [...]

    Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

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    Springer Science and Business Media LLC, 2016

    Published in: Human Genetics

  5. Mlynarski, Elisabeth E.; Sheridan, Molly B.; Xie, Michael; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Gai, Xiaowu; Chow, Eva W.C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; [...]

    Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

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    Elsevier BV, 2015

    Published in: The American Journal of Human Genetics

  6. Herman, Sean B.; Guo, Tingwei; McGinn, Donna M. McDonald; Blonska, Anna; Shanske, Alan L.; Bassett, Anne S.; Chow, Eva W.C.; Bowser, Mark; Sheridan, Molly; Beemer, Frits; Devriendt, Koen; Swillen, Ann; Breckpot, Jeroen; Digilio, M. Cristina; Marino, Bruno; Dallapiccola, Bruno; Carpenter, Courtney; Zheng, Xin; Johnson, Jacob; Chung, Jonathan; Higgins, Anne Marie; Philip, Nicole; Simon, Tony; Coleman, Karlene; [...]

    Overt cleft palate phenotype andTBX1genotype correlations in velo‐cardio‐facial/DiGeorge/22q11.2 deletion syndrome patients

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    Wiley, 2012

    Published in: American Journal of Medical Genetics Part A

  7. Guo, Tingwei; McDonald-McGinn, Donna; Blonska, Anna; Shanske, Alan; Bassett, Anne S.; Chow, Eva; Bowser, Mark; Sheridan, Molly; Beemer, Frits; Devriendt, Koen; Swillen, Ann; Breckpot, Jeroen; Digilio, Maria C.; Marino, Bruno; Dallapiccola, Bruno; Carpenter, Courtney; Zheng, Xin; Johnson, Jacob; Chung, Jonathan; Higgins, Anne Marie; Philip, Nicole; Simon, Tony J.; Coleman, Karlene; Heine-Suner, Damian; [...]

    Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients

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    Hindawi Limited, 2011

    Published in: Human Mutation