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Zirn, Birgit [Author]

Die genetische Sprechstunde : ein Ratgeber mit Beispielen aus der Praxis

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Heidelberg: Steinkopff, 2009
Zirn, Birgit [Editor]; Mehnert, Karl [Editor]

Handbuch für die genetische Sprechstunde

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Berlin; Heidelberg: Springer, [2017]

Published in: SpringerLink ; Bücher - Springer eBook Collection ; Medicine
Zirn, Birgit [Author]; Mehnert, Karl [Author]

Guide for Genetic Consultation

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Cham: Springer, 2019

Published in: Springer eBooks ; Medicine
Bach, Veronika Franziska [Author] ; Zirn, Birgit [Degree supervisor]; Bauerschmitz, Gerd-Johannes [Degree supervisor]; Schön, Margarete [Degree supervisor]

Pränataldiagnostik zur Detektion chromosomaler Aberrationen: Wandel in der Anwendung invasiver und nicht-invasiver Methoden = Prenatal diagnostics for detection chromosomal aberrations: changes in the use of invasive and non-invasive methods

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Göttingen, 2022
Klein, Nina [Author] ; Zirn, Birgit [Degree supervisor]; Zoll, Barbara [Other]; Schön, Margarete [Other]

Array-CGH bei Kindern mit Entwicklungsstörung oder geistiger Behinderung: Bei welcher Konstellation finden sich gehäuft klinisch relevante Chromosomenaberrationen?

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Göttingen, 2016
Borchers, Maike [Author] ; Zirn, Birgit [Degree supervisor]; Zoll, Barbara [Other]; Schön, Margarete [Other]

Auswirkung einer genetischen Diagnose auf die Lebensqualität von Eltern behinderter Kinder

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2016
Harr, Claudia Mareike [Author] ; Klintschar, Michael [Degree supervisor]; Klintschar, Michael [Other]; Zirn, Birgit [Other]

Genetische Polymorphismen der mtDNA als Risikofaktoren für das SIDS (Sudden Infant Death Syndrome)

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2013
Zirn, Birgit [Author]; Bernbeck, Ulrich [Author]; Alt, Kerstin [Author]; Oeffner, Frank [Author]; Gerhardinger, Andreas [Author]; Has, Cristina [Author]

Rothmund–Thomson syndrome type 1 caused by biallelic ANAPC1 gene mutations

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Hoboken, NJ: Wiley, 2021

Published in: Skin health and disease ; 1, 1 (2021), e12
Frommherz, Leonie [Author]; Krause, Alexandra [Author]; Kopp, Julia [Author]; Hotz, Alrun Göntje [Author]; Hübner, Stefanie [Author]; Reimer-Taschenbrecker, Antonia [Author]; Casetti, Federica [Author]; Zirn, Birgit [Author]; Fischer, Judith [Author]; Has, Cristina [Author]

High rate of self‐improving phenotypes in children with non‐syndromic congenital ichthyosis: case series from south‐western Germany

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Oxford: Wiley-Blackwell, 2021

Published in: Journal of the European Academy of Dermatology and Venereology ; 35, 11 (2021), 2293-2299
Mitter, Diana [Author]; Pringsheim, Milka [Author]; Kaulisch, Marc [Author]; Plümacher, Kim Sarah [Author]; Schröder, Simone [Author]; Warthemann, Rita [Author]; Abou Jamra, Rami [Author]; Baethmann, Martina [Author]; Bast, Thomas [Author]; Büttel, Hans-Martin [Author]; Cohen, Julie S. [Author]; Conover, Elizabeth [Author]; Courage, Carolina [Author]; Eger, Angelika [Author]; Fatemi, Ali [Author]; Grebe, Theresa A. [Author]; Hauser, Natalie S. [Author]; Heinritz, Wolfram [Author]; Helbig, Katherine L. [Author]; Heruth, Marion [Author]; Huhle, Dagmar [Author]; Höft, Karen [Author]; Karch, Stephanie [Author]; Kluger, Gerhard [Author]; [...]

FOXG1 syndrome : genotype–phenotype association in 83 patients with FOXG1 variants

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2018

Published in: Genetics in medicine ; 20(2018), 1, Seite 98-108
Zirn, Birgit [Author]

Expressions- und Mutationsanalysen in kindlichen Wilms-Tumoren

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Harr, Claudia Mareike [Author] ; Klintschar, Michael [Degree supervisor]; Zirn, Birgit [Degree supervisor]

Genetische Polymorphismen der mtDNA als Risikofaktoren für das SIDS (Sudden Infant Death Syndrome)

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2015
Shoukier, Moneef [Author] ; Engel, Wolfgang [Degree supervisor]; Zirn, Birgit [Degree supervisor]

Zur molekularen und funktionellen Charakterisierung von Mutationen in den SPG4- und SPG7-Genen

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2011
Bach, Veronika Franziska [Author] ; Zirn, Birgit [Degree supervisor]; Bauerschmitz, Gerd-Johannes [Other]; Schön, Margarete [Other]

Pränataldiagnostik zur Detektion chromosomaler Aberrationen: Wandel in der Anwendung invasiver und nicht-invasiver Methoden

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2022
Klein, Nina [Author] ; Zirn, Birgit Apl [Degree supervisor]; Zoll, Barbara [Other]; Schön, Margarete [Other]

Array-CGH bei Kindern mit Entwicklungsstörung oder geistiger Behinderung: Bei welcher Konstellation finden sich gehäuft klinisch relevante Chromosomenaberrationen?

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2017
Borchers, Maike [Author] ; Zirn, Birgit [Degree supervisor]; Zoll, Barbara [Other]; Schön, Margarete [Other]

Auswirkung einer genetischen Diagnose auf die Lebensqualität von Eltern behinderter Kinder

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016
Zirn, Birgit; Wittmann, Stefanie; Gessler, Manfred

Novel Familial WT1 Read-Through Mutation Associated With Wilms Tumor and Slow Progressive Nephropathy

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Elsevier BV, 2005

Published in: American Journal of Kidney Diseases, 45 (2005) 6, Seite 1100-1104
Moog, Ute; Felbor, Ute; Has, Cristina; Zirn, Birgit

Disorders Caused by Genetic Mosaicism

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Deutscher Arzte-Verlag GmbH, 2020

Published in: Deutsches Ärzteblatt international (2020)
Zirn, Birgit; Samans, Birgit; Wittmann, Stefanie; Pietsch, Thorsten; Leuschner, Ivo; Graf, Norbert; Gessler, Manfred

Target genes of the WNT/β‐catenin pathway in Wilms tumors

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Wiley, 2006

Published in: Genes, Chromosomes and Cancer, 45 (2006) 6, Seite 565-574
Zirn, Birgit; Samans, Birgit; Spangenberg, Christian; Graf, Norbert; Eilers, Martin; Gessler, Manfred

All-trans retinoic acid treatment of Wilms tumor cells reverses expression of genes associated with high risk and relapse in vivo

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Springer Science and Business Media LLC, 2005

Published in: Oncogene, 24 (2005) 33, Seite 5246-5251

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