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Qualitätsförderungsprogramm des TGF
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Janetschek, Kevin Rostasy, Sabine Scholl-Bürgi, Sibylle Zotter, Gerd Utermann, Johannes. Zschocke, Dieter Kotzot, Edda Haberlandt.
Jubiläumsfonds der Österreichischen Nationalbank - myPoint
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Untersuchung balancierter Chromosomenaberrationen (Dieter KOTZOT, Institut für Medizinische Biologie und Humangenetik) Effekte unterschiedlicher Antipsychotika der
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Dieter Kotzot - Düsseldorf (Städt. Gemeinschaftshauptschule...
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Dieter Kotzot ist Mitglied bei StayFriends und hat bis diese Schule besucht: Städt. Gemeinschaftshauptschule Emil-Barth-Straße.
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Dieter Kotzot is on Facebook. Join Facebook to connect with Dieter Kotzot and others you may know. Facebook gives people the power to share and makes the world more
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Profile der Personen mit dem Namen Dieter Kotzot auf Facebook anzeigen Tritt Facebook bei, um dich mit Dieter Kotzot und anderen Nutzern, die du vielleicht ...
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Journal of Pediatrics, The - Vol n° 4 - EM consulte
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Le site de référence en informations médicales et paramédicales - EM|consulte
Bücher
Congenital Thoracic Wall Deformities: Diagnosis, Therapy and Current...
books.google.de
These congenital deformities, funnel or keel chest deformities, as well as Poland syndromes, affect a small group of patients who suffer from aesthetic rather...
Vitamin E und Acetylsalicylsäure, Vergleich ihrer Wirkung auf...
books.google.ru
Dieter Kotzot pages. 0 Reviewshttp://books.google.com/books/about/Vitamin_E_und_Acetylsalicyls%C3%A4ure_Vergle.html?id=vwhBngEACAAJ ...
Dokumente zum Namen
EBSCOhost | | Don't miss patients with atypical FMR1...
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Johannes Zschocke & Dieter Kotzot. Received: 1 April Revised: 27 June Accepted: 27 June Published online: 17 July
Mental retardation, developmental delay, and partial psychomotor...
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6 # $ 4 $ # = =
EBSCOhost | | Paternal meiotic origin of der(21;21)(q10;q10)...
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Dieter Kotzot and Albert Schinzel. Institut für Medizinische Genetik, Universität Zürich, Switzerland. Mosaicism for a derivative 21, der(21;21)(q10;q10), is a rare ...
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate...
www.deepdyve.com
Stefanie Belet. •. Jelle Verbeeck. •. Nathalie Fieremans. •. Maureen Holvoet. •. Jodie Vento. •. Ana Spreiz. •. Dieter Kotzot. •. Edda Haberlandt.
Wissenschaftliche Veröffentlichungen
Trends in Molecular Medicine | Special Issue: Nurturing the Next...
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Mosaicism and uniparental disomy in prenatal diagnosis. Review article: Pages Thomas Eggermann, Lukas Soellner, Karin Buiting, Dieter Kotzot.
Reviewer acknowledgement | Molecular Cytogenetics | Full Text
molecularcytogenetics.biomedcentral.com
Benjamin Kamien. Australia. Elena Kirillova. Russia. Genevieve Konopka. United States. Nadezda Kosyakova. Germany. Dieter Kotzot. Austria.
Scientists identify gene predisposing to artery-damaging disease
www.sciencedaily.com
A genetic discoverycould help explain a cause of a mysterious artery-damaging disease that may affect up to an estimated 5 million Americans and often strikes...
OPUS 4 | Elevated heart rate triggers action potential alternans and...
publikationen.ub.uni-frankfurt.de
Ulrich Schweigmann, Peter Biliczki, Rafael J. Ramirez, Christoph Marschall, Ina Takac, Ralf P. Brandes, Dieter Kotzot, Zenawit Girmatsion, ...
Veröffentlichungen allgemein
A new molecular approach to investigate origin and formation of...
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Benno RÎthlisberger, Albert Schinzel & Dieter Kotzot. Institute of Medical Genetics, University of ZÏrich, RÌ, CH ZÏrich, Switzerland;. Tel: ‡ ‡ 41-(0)1 ...
Don’t miss patients with atypical FMR1 mutations: dysmorphism and...
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Johannes Zschocke & Dieter Kotzot. Received: 1 April Revised: 27 June Accepted: 27 June © Springer-Verlag Berlin Heidelberg
Uniparentale Disomien und Mosaike | SpringerLink
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(1); Dieter Kotzot (2). Author Affiliations. 1. Institut für Humangenetik, Universitätsklinikum der RWTH Aachen, Aachen ...
Oalib search
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Abstract: Hyperparathyroidism Jaw-Tumour Syndrome (HPT-JT) is characterized by primary hyperparathyroidism (PHPT), ...
Artikel & Meinungen
Disruption of EXOC6B in a patient with developmental delay, epilepsy,...
www.nature.com
Short Report
Sonstiges
Infertility: Kotzot, Dieter - Expertscape.com
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Dieter Kotzot has special expertise in Infertility
DFP-Kalender
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PD Dr. Dieter Kotzot . Referenten. Dieter Kotzot - Medizinische Genetik. Interessenskonflikte.
Kotzot - Names Encyclopedia
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Given names Josef Kotzot (2) Anna Kotzot (2) Hubert Kotzot (2) Dieter Kotzot (2) Stefan Kotzot (1) Ulrich Kotzot (1) Reinhard Kotzot (1) Ulrike Kotzot (1)
Kotzot Namensbedeutung und -herkunft
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Anna Kotzot (2) Hubert Kotzot (2) Dieter Kotzot (2) Stefan Kotzot (1) Ulrich Kotzot (1) Reinhard Kotzot (1) Ulrike Kotzot (1) Bernhard Kotzot (1) Herbert Kotzot (1)
Complex and segmental uniparental disomy (UPD): review and lessons...
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Author(s): Dieter Kotzot . Source: Journal of Medical Genetics. Document Type: Article. Article Preview : Abstract Objective--To review all cases with segmental ...
Deletions of the RUNX2 Gene are present in about 10% of Individuals...
hal.archives-ouvertes.fr
... Haase 7 Juergen Kohlhase 8Dieter Kotzot 9 Andrew Lane 10 Min Ae Lee-Kirsch 11 Susanne Morlot 12 Marleen Eh Simon 13 Elisabeth Steichen-Gersdorf
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
pure.au.dk
... der Knaap}, {Marjo S} and Kornberg, {Andrew J} and Dieter Kotzot and Wilfried Kratzer and Didier Lacombe and Lieven Lagae and Landrieu, {Pierre Georges} ...
PLOS ONE: Elevated Heart Rate Triggers Action Potential Alternans and...
journals.plos.org
PLOS ONE: an inclusive, peer-reviewed, open-access resource from the PUBLIC LIBRARY OF SCIENCE. Reports of well-performed scientific studies from all...
Chromosomal microaberrations in patients with epilepsy, intellectual...
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Abstract
Epilepsy is a common finding in patients with chromosomal macro‐ and micro‐rearrangements but only few aberrations show a constant pattern of...
Papers in the shared collection Nephrocalcinosis/Medullary sponge...
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Edgar Meusburger, Axel Mündlein, Emanuel Zitt, Barbara Obermayer-Pietsch, Dieter Kotzot, Karl Lhotta. Idiopathic infantile hypercalcaemia ...
Journal of Pediatric Nursing - Related By Results
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Dieter Kotzot, Anton H. Schwabegger, Review article, October 2009, Journal of Pediatric Surgery Vol. 44, Issue 10, Pages Pediatric leukemia ...
Don't miss patients with atypical FMR1 mutations: dysmorphism and...
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Edda Haberlandt, Sibylle Zotter, Martina Witsch-Baumgartner, Johannes Zschocke, Dieter Kotzot. European Journal of Pediatrics July
Single nucleotide polymorphism array analysis in men with idiopathic ...
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Email the author M.D. Dieter Kotzot · Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome.
Mental retardation, developmental delay, and partial psychomotor...
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Mental retardation, developmental delay, and partial psychomotor deficits in maternal uniparental disomy 7. more. COLLAPSE. Dieter Kotzot · Details · Authors ...
Single nucleotide polymorphism array analysis in men with idiopathic...
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Anne Frühmesser, Peter H Vogt, Jutta Zimmer, Martina Witsch-Baumgartner, Christine Fauth, Johannes Zschocke, Germar-Michael Pinggera, Dieter Kotzot.
Uniparentale Disomien und Mosaike
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Dieter Kotzot. Medizinische Universität Innsbruck, Sektion Humangenetik, Department für Medizinische Genetik, Molekulare und Klinische Pharmakologie, Innsb ...
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate...
read.qxmd.com
... Stefanie Belet, Jelle Verbeeck, Nathalie Fieremans, Maureen Holvoet, Jodie Vento, Ana Spreiz, Dieter Kotzot, Edda Haberlandt, Jill Rosenfeld, Joris Andrieux, ...
Enrico Bertini - Publications List
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... Yong-Hui Jiang, Sarina G Kant, Amy Kao, Mary D King, Helen M Kingston, Joerg Klepper, Marjo S van der Knaap, Andrew J Kornberg, Dieter Kotzot, Wilfried
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