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Not only the gene itself, its abnormal regula | EurekAlert!
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A specific gene is particularly frequently involved in the development of short stature. Researchers in Heidelberg have now discovered that sequences of...
Warum Kinder nicht mehr wachsen
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Jianjun Chen, Gabriele Wildhardt, Zilin Zhong, Ralph Roeth, Birgit Weiss, Daniela Steinberger, Jochen Decker, Werner F Blum, Gudrun A Rappold. Enhancer mutations of the
Not Just The Gene - Abnormal SHOX Regulation Implicated In Short...
www.science20.com
Article: Jianjun Chen, Gabriele Wildhardt, Zilin Zhong, Ralph Roeth, Birgit Weiss, Daniela Steinberger, Jochen Decker, Werner F Blum and Gudrun A Rappold, 'Enhancer
Netzwerk-Profile
LinkedIn: Dr. Gabriele Wildhardt | LinkedIn
Dr. Gabriele Wildhardts berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Dr. Gabriele ...
LinkedIn: Gabriele Wildhardt | LinkedIn
Gabriele Wildhardts berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Gabriele Wildhardt ...
LinkedIn: Dr. Gabriele Wildhardt | LinkedIn
Sehen Sie sich das berufliche Profil von Dr. Gabriele Wildhardt (Deutschland) auf LinkedIn an. LinkedIn ist das weltweit größte professionelle Netzwerk, das ...
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Spectrum of novel mutations found in Waardenburg syndrome types 1 and...
bmjopen.bmj.com
Gabriele Wildhardt bio.logis Center for Human Genetics, Frankfurt am Main, Germany PubMed articlesGoogle scholar articles; Birgit Zirn Department of ...
Table of contents | BMJ Open
bmjopen.bmj.com
Gabriele Wildhardt, Birgit Zirn, Luitgard M Graul-Neumann, Juliane Wechtenbruch, Markus Suckfüll, Annegret Buske, Axel Bohring, Christian Kubisch, Stefanie ...
Firmen-Mitarbeiter
Gabriele Wildhardt - Member - ClinGen | Clinical Genome Resourceclinicalgenome.org › people › staff › wildhardt-3593
clinicalgenome.org
Gabriele Wildhardt. Working Groups & Expert Panels. Low Penetrance/Risk Allele · About Us About ClinGen ClinGen & ClinVar Partnership ClinGen, ...
Kommissionen | GfH - Deutsche Gesellschaft für Humangenetik e.V.
gfhev.de
Dr. rer. nat. Gabriele Wildhardt, Frankfurt/M. Dr. rer. nat. Frank Oeffner, Neu-Ulm. GfH-Delegierte für die (Fort-)Entwicklung von GfH-Leitlinien (LL)
Private Homepages
Infevers - Contact
infevers.umai-montpellier.fr
You have a question, a suggestion regarding this variant (G136R) ? Please, fill this fields to send an e-mail to Gabriele WILDHARDT. For your information, a ...
Dokumente zum Namen
Gabriele Wildhardt - Academia.edu
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Waardenburg syndrome type I with heterochromia iridis and...
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... Preeti Singh, Renate Vöhringer, Timm Goecke, Ertan Mayatepek, Thomas Ruzicka, Gabriele Wildhardt, Thomas Meissner, Roland Kruse.
Utility of MLPA in deletion analysis of GCH1 in dopa-responsive...
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ERRATUM Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia Daniela Steinberger & Jutta Trübenbach & Birgit Zirn & Barbara Leube &…
Wissenschaftliche Veröffentlichungen
Spectrum of novel mutations found in Waardenburg syndrome types 1 and...
epub.ub.uni-muenchen.de
Wildhardt, Gabriele und Zirn, Birgit und Graul-Neumann, Luitgard M. und Wechtenbruch, Juliane und Suckfuell, Markus und Buske, ... Abstract. Objectives: Till …
Preisträgerarchiv - Science4Life : Science4Life
www.science4life.de
Ivar Roots Prof. Dr. med. Daniela Steinberger Dr. rer. medic. Bernd Timmermann Dipl. Biol. Jutta Trübenbach Dr. rer.nat. Gabriele Wildhardt. Kontaktperson Prof.
Short Stature: Both A Specific Gene, And Its Abnormal Regulation, Can...
www.sciencedaily.com
A specific gene is particularly frequently involved in the development of short stature. Researchers in Germany have now discovered that sequences of genetic...
Veröffentlichungen allgemein
Mutations in the PDS gene in German families with Pendred's syndrome:...
www.pubfacts.com
Pendred's syndrome, an autosomal-recessive condition characterized by...
Artikel & Meinungen
Дневник garrilazaleksan : LiveInternet - Российский Сервис...
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Дневник garrilazaleksan Виртуальный дневник garrilazaleksan
A comparative study of germline BRCA1 and BRCA2 mutation screening...
www.nature.com
Dr Gabriele Wildhardt, bio.logis Center for Human Genetics, Frankfurt am Main, Germany. Dr Julian Nevado, Genomics of INGEMM-HULP, ...
CFTR molecular screening - HUM-MOLGEN
hum-molgen.org
Dr. Gabriele Wildhardt. IP: Wildhardt Member : posted :26 AM quote: Originally posted by mtm: Is there anyone interested on mutation …
Sonstiges
Suchmaschine BASE (Bielefeld Academic Search Engine): Trefferliste
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Ergebnis Ihrer Suche im BASE.
Kommissionen des BVDH e.V. | BVDH
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Frau Dr. rer. nat. Gabriele Wildhardt, Frankfurt a.M. Herr PD Dr. rer. physiol. Frank Oeffner, Neu-Ulm. Stellvertreterin: Frau Prof. Dr. med. Ursula Froster, Zwenkau .
Enhancer mutations of the SHOX gene as a frequent cause of short...
hal.archives-ouvertes.fr
Mutations and deletions of the homeobox transcription factor gene are known to cause short stature. We have analyzed SHOX enhancer regions in a large cohort of...
Infevers - Details
infevers.umai-montpellier.fr
Reference, Gabriele Wildhardt Personal communication. Contributed by, Gabriele WILDHARDT. Comment, The patient carries also the mutation c.1129G>A (p.
LIDSEN Publishing Inc.丨The Open Access Publisher
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LIDSEN series of journals are published by LIDSEN Publishing Inc, a non-profit scholarly Open Access publisher focused on biological, biomedical and medical...
OBM Genetics | German Guidelines for Molecular Genetic Diagnostic...
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We present, on behalf of the German Society of Human Genetics, guidelines for molecular genetic diagnostics with high throughput technology, for example using...
Altmetric – Spectrum of novel mutations found in Waardenburg syndrome...
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Gabriele Wildhardt, Birgit Zirn, Luitgard M Graul-Neumann, Juliane Wechtenbruch, Markus Suckfüll, Annegret Buske, Axel Bohring, Christian Kubisch, Stefanie ...
Warum Kinder nicht mehr wachsen
www.gesundheitsindustrie-bw.de
Literatur:Jianjun Chen, Gabriele Wildhardt, Zilin Zhong, Ralph Roeth, Birgit Weiss, Daniela Steinberger, Jochen Decker, Werner F Blum, Gudrun A Rappold.
S1 Leitlinie: Molekulargenetische Diagnostik mit...
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Angewandte Genomik und CENTOGENE AG, Rostock (federführend) Gabriele Wildhardt, ...
Altmetric – Four New Cases of Congenital Secondary Hypothyroidism due...
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Guntram Borck, A. Kemal Topaloglu, Eckhard Korsch, Ursula Martiné, Gabriele Wildhardt, Neslihan Onenli-Mungan, Bilgin Yuksel, Ulrich Aumann, Gerhard ...
Eigentümerinteresse an Arzneimitteln/Medizinprodukten (z. B. Patent,...
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... European Society of Human Genetics, Deutsche Krebsgesellschaft Dr. Gabriele Wildhardt, GfH, BVDH, DGKL bio.logis GmbH Otto-von-Guericke- Universität ...
(PDF) Hypochondroplasie, Achondroplasie und thanatophore Dysplasie...
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Gabriele Wildhardt + 5 · Gabriele Wildhardt. Monika Hilbert. K. Hilbert. J. Spranger. Andreas Winterpacht. Bernhard Zabel. Download with Google Download with ...
Utility of MLPA in deletion analysis of GCH1 in - ProQuestwww.proquest.com › scholarly-journals › docview
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Barbara Leube & Gabriele Wildhardt & Ulrich Mller. Published... Show less. You have requested "on-the-fly" machine translation of selected content from our ...
Molecular Genetic Diagnosis of the gene SHOX (short stature homeobox)...
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J ed Genet ay;44(5): Jianjun Chen, Gabriele Wildhardt, Zilin Zhong, Ralph Röth, Birgit Weiss, Daniela Steinberger, Jochen Decker, Werner F. Blum, Gudrun ...
Molekulargenetische Diagnostik des Kleinwuchses. Genanalysen bei...
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Daniela Steinberger Dr. rer. nat. Gabriele Wildhardt Dipl. Biol. Jutta Trübenbach Dr. phil. Maike Post akkreditiert durch: College of merican Pathologists (CP).
Utility of MLPA in deletion analysis of GCH1 in dopa PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Authors. Daniela Steinberger , Jutta Trübenbach, Birgit Zirn, Barbara Leube, Gabriele Wildhardt, Ulrich Müller. Affiliation. 1 Institut für Humangenetik, ...
Low Penetrance/Risk Allele - ClinGen | Clinical Genome Resource
clinicalgenome.org
Emily Qian, MS, CGC. Timo Dereani. Natalie Vena. Alissa Keegan, MD, PhD. Daniela Steinberger. Sabine Naumann. Gabriele Wildhardt. Maria Korte ...
Martine frising wiltz
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2 Martine Frising, Gabriele Wildhardt, Lars Frisch MARTINE FRISING published 4 Research Articles on Aspergillosis Astigmatism Choroid Neoplasms ...
Monogen erbliche Formen des Diabetes mellitus - PDF Kostenfreier...
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366 Schwerpunkt Monogen erbliche Formen des Diabetes mellitus Genetische Diagnostik Albert Driesel 1,2, Gabriele Wildhardt 1, Daniela Steinberger 1,
Mutation screening for the prothrombin variant G20210A by melting ...www.semanticscholar.org › paper › Mutation-screen...
www.semanticscholar.org
· author={C Wylenzek and Jutta Tr{\"u}benbach and Peter Gohl and Gabriele Wildhardt and Stephan A Alkins and M. Bardett Fausett and Jeremy ...
Verwandte Suchanfragen zu Gabriele Wildhardt
| Jutta Trübenbach Axel Bohring Ralph Roeth | Annegret Buske Juliane Wechtenbruch Birgit Weiss | Jochen Decker Markus Suckfüll Birgit Zirn |
Personen Vorname "Gabriele" (39779) Name "Wildhardt" (14) |
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