1
0
0
News
Inhaltsverzeichnis
www.aerzteblatt.de
— DEUTSCHES ÄRZTEBLATT Klinik und Genetik der tuberösen Sklerose Hans-Dieter Rott und Raimund Fahsold Die tuberöse Sklerose ist ... › archiv › inhalt
Interessen
Issue: The American Journal of Human GeneticsCell Press
www.cell.com
Raimund Fahsold,; Werner Leistner,; Dieter Kaufmann,; Winfrid Krone. Stop mutations are known to disrupt gene function in different ways. They both give rise to ... Raimund Fahsold,; Werner Leistner,; Dieter Kaufmann,; Winfrid Krone. Stop mutations are known to disrupt gene function in different ways. They both give rise to ...
Minor Lesion Mutational Spectrum of the Entire NF1 Gene ...Cell Press
www.cell.com
von R Fahsold · · Zitiert von: 398 — Raimund Fahsold *. Author Footnotes. * These authors contributed equally to this work. Raimund Fahsold. Footnotes. * These authors contributed equally to this ... von R Fahsold · · Zitiert von: 398 — Raimund Fahsold *. Author Footnotes. * These authors contributed equally to this work. Raimund Fahsold. Footnotes. * These authors contributed equally to this ...
Nearby Stop Codons in Exons of the Neurofibromatosis Type 1 Gene Are...
www.cell.com
Sven Hoffmeyer 1, Peter Nürnberg 2, Heide Ritter 2, Raimund Fahsold 4, Werner Leistner 3, Dieter Kaufmann 1 and Winfrid Krone Abteilung Humangenetik
Ausbildung
American Journal of Medical Genetics Part AScholars Portal Journals
journals.scholarsportal.info
Authors. Christian Thiel · ORCID ID · Martin Wilken · Martin Zenker · Heinrich Sticht · Raimund Fahsold · Gabriele-Charlotte Gusek-Schneider · Anita Rauch ... Authors. Christian Thiel · ORCID ID · Martin Wilken · Martin Zenker · Heinrich Sticht · Raimund Fahsold · Gabriele-Charlotte Gusek-Schneider · Anita Rauch ...
Journal of NeurologyScholars Portal Journals
journals.scholarsportal.info
Raimund Fahsold · Holger Grehl · Detlef Claus. Source Information. February 1995, Volume242(Issue2)Pages, p.99To Abstract. An unstable DNA sequence of a ... Raimund Fahsold · Holger Grehl · Detlef Claus. Source Information. February 1995, Volume242(Issue2)Pages, p.99To Abstract. An unstable DNA sequence of a ...
Bücher
Raimund Fahsold | University of Erlangen-NurembergAI Chat for scientific PDFs
typeset.io
Raimund Fahsold is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: CD3 & Neurology. Raimund Fahsold is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: CD3 & Neurology.
Azospirillum III: Genetics · Physiology · Ecology ...google.de
books.google.de
... Raimund Fahsold , Mahavir Singh and Walter Klingmüller Lehrstuhl für Genetik , Universität Bayreuth Universitätstr , D Bayreuth , FRG Summary ...
Egyetemi Könyvtár - Böngészés - szerző: "Raimund Fahsold" - DEA
dea.lib.unideb.hu
Egyetemi Könyvtár - Böngészés - szerző: "Raimund Fahsold" A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. Vagy adja meg az első pár betűt:.
Raimund Fahsold | XanEdu Customization Platform
www.academicpub.com
Author: Raimund Fahsold. Results. Fatal glioblastoma multiforme in a patient with neurofibromatosis type I: the dilemma of systematic medical follow-up.
Dokumente zum Namen
American Journal of Medical Genetics Part AWiley Online Library
onlinelibrary.wiley.com
... Raimund Fahsold, Hartmut Schmidt, Katrin Hoffmann and Eberhard Passarge A: New Lethal Skeletal Dysplasia with Dandy-Walker Malformation Raimund Fahsold, Hartmut Schmidt, Katrin Hoffmann and Eberhard Passarge A: New Lethal Skeletal Dysplasia with Dandy-Walker Malformation ...
Syndroms im KindesDigitale Bibliothek Thüringen
www.db-thueringen.de
von UE Müller — Raimund Fahsold und das Team des molekulargenetischen Labors der Gemeinschaftspraxis Prager/Junge (-. 40, Dresden) für die Durchführung ... von UE Müller — Raimund Fahsold und das Team des molekulargenetischen Labors der Gemeinschaftspraxis Prager/Junge (-. 40, Dresden) für die Durchführung ...
Independent NF1 and PTPN11 mutations in a family with ...Wiley Online Library
onlinelibrary.wiley.com
von C Thiel · · Zitiert von: 71 — Raimund Fahsold,. Raimund Fahsold. Private Clinic B. Prager & A. Junge, Dresden, Germany. Search for more papers by this author · Gabriele ... von C Thiel · · Zitiert von: 71 — Raimund Fahsold,. Raimund Fahsold. Private Clinic B. Prager & A. Junge, Dresden, Germany. Search for more papers by this author · Gabriele ...
Unusual Radiological Presentation of Tuberous Sclerosis ...Sage Journals
journals.sagepub.com
Raimund Fahsold, MD. Gemeinschaftspraxis B. Prager & A. Junge, Dresden, Germany. View all articles by this author. Min Ae Lee-Kirsch, MD. Children's Hospital ... Raimund Fahsold, MD. Gemeinschaftspraxis B. Prager & A. Junge, Dresden, Germany. View all articles by this author. Min Ae Lee-Kirsch, MD. Children's Hospital ...
Wissenschaftliche Veröffentlichungen
An intronic splice site alteration in combination with a large ...ScienceDirect.com
www.sciencedirect.com
von F Boschann · · Zitiert von: 7 — Raimund Fahsold: Resources. Denise Horn: Resources, Writing - review & editing. Luitgard M. Graul-Neumann: Conceptualization,. Declaration of competing ... von F Boschann · · Zitiert von: 7 — Raimund Fahsold: Resources. Denise Horn: Resources, Writing - review & editing. Luitgard M. Graul-Neumann: Conceptualization,. Declaration of competing ...
The American Journal of Human Genetics | Vol 66, Issue 3, Pages i-ii,...
www.sciencedirect.com
Raimund Fahsold, Sven Hoffmeyer, Claudia Mischung, Christoph Gille, ... Peter Nürnberg. Pages : Download PDF. Article preview. select article An ...
The Human Genome Puzzle — the Role of Copy Number Variation...:...
www.ingentaconnect.com
Raimund Fahsold. 7. , Marianne Volleth. 8 and. Anja Weise*. ,1. 1Jena University Hospital, Institute of Human Genetics and Anthropology, Jena, Germany; ...
Untersuchungen zur molekularen Genetik der Stickstoffixierung in...
eref.uni-bayreuth.de
Titelangaben Fahsold, Raimund: Untersuchungen zur molekularen Genetik der Stickstoffixierung in Azospirillum lipoferum: Klonierung, Kartierung u.
Veröffentlichungen allgemein
Nearby Stop Codons in Exons of the Neurofibromatosis ...CORE
core.ac.uk
von S Hoffmeyer · · Zitiert von: 73 — ... Raimund Fahsold,4 Werner Leistner,3. Dieter Kaufmann,1 and Winfrid Krone1. 1Abteilung Humangenetik, Universität Ulm, Ulm; 2Institut für Medizinische Genetik ... von S Hoffmeyer · · Zitiert von: 73 — ... Raimund Fahsold,4 Werner Leistner,3. Dieter Kaufmann,1 and Winfrid Krone1. 1Abteilung Humangenetik, Universität Ulm, Ulm; 2Institut für Medizinische Genetik ...
Azospirillum III: Genetics · PhysiologySpringer
link.springer.com
von W Klingmüller · Zitiert von: 13 — Cosmid Cloning of Nitrogenase Structural Genes of Azospirillum Lipoferum. Raimund Fahsold, Mahavir Singh, Walter Klingmüller. Pages Download chapter PDF ... von W Klingmüller · Zitiert von: 13 — Cosmid Cloning of Nitrogenase Structural Genes of Azospirillum Lipoferum. Raimund Fahsold, Mahavir Singh, Walter Klingmüller. Pages Download chapter PDF ,99 $
Cosmid Cloning of Nitrogenase Structural Genes ...Springer
link.springer.com
von R Fahsold · · Zitiert von: 16 — Raimund Fahsold, ... Authors and Affiliations. Lehrstuhl für Genetik, Universität BayreuthD-8580, Bayreuth, Germany. Raimund Fahsold, ... von R Fahsold · · Zitiert von: 16 — Raimund Fahsold, ... Authors and Affiliations. Lehrstuhl für Genetik, Universität BayreuthD-8580, Bayreuth, Germany. Raimund Fahsold, ...
Sonstiges
Nearby Stop Codons in Exons of the Neurofibromatosis ...SlidePlayer
slideplayer.com
Sven Hoffmeyer, Peter Nürnberg, Heide Ritter, Raimund Fahsold, Werner Leistner, Dieter Kaufmann, Winfrid Krone The American Journal of Human Genetics Volume ... Sven Hoffmeyer, Peter Nürnberg, Heide Ritter, Raimund Fahsold, Werner Leistner, Dieter Kaufmann, Winfrid Krone The American Journal of Human Genetics Volume ...
Raimund Fahsold's scientific contributionsResearchGate
www.researchgate.net
Raimund Fahsold's 7 research works with 77 citations and 543 reads, including: An intronic splice site alteration in combination with a large deletion ... Raimund Fahsold's 7 research works with 77 citations and 543 reads, including: An intronic splice site alteration in combination with a large deletion ...
32 Treffer für "Ulrich Sander" im HandelsregisterCompanyhouse
www.companyhouse.de
Verbundene Manager: Raimund Fahsold, Sabine Lorenz, Dan-Christian Mentel · Ulrich H. Sander. Inaktiv. 1. Frühere Verbindungen: Eisenführ, Speiser & Partner ... Verbundene Manager: Raimund Fahsold, Sabine Lorenz, Dan-Christian Mentel · Ulrich H. Sander. Inaktiv. 1. Frühere Verbindungen: Eisenführ, Speiser & Partner ...
A variable combination of features of Noonan syndrome ...Academia.edu
www.academia.edu
... Raimund Fahsold,2 and Anita Rauch1* 1 Institute of Human Genetics, University Erlangen-Nuremberg, Erlangen, Germany 2 Clinic for Medical Genetics, Dresden Raimund Fahsold,2 and Anita Rauch1* 1 Institute of Human Genetics, University Erlangen-Nuremberg, Erlangen, Germany 2 Clinic for Medical Genetics, Dresden ...
Advance Search | Bentham ScienceEurekaselect
www.eurekaselect.com
... Raimund Fahsold, Marianne Volleth, Anja Weise. Phase II Drug Metabolism and Individualized Drug Therapy: A Focus on Functional Genetic Variation in UDP Raimund Fahsold, Marianne Volleth, Anja Weise. Phase II Drug Metabolism and Individualized Drug Therapy: A Focus on Functional Genetic Variation in UDP ...
Altersabhängige Merkmalsausprägung des MarfanDocPlayer.org
docplayer.org
Raimund Fahsold in Dresden vorgenommen. Die direkte genomische Sequenzierung erfolgte in folgenden Schritten: zunächst wurden die Proben in einem ersten ... Raimund Fahsold in Dresden vorgenommen. Die direkte genomische Sequenzierung erfolgte in folgenden Schritten: zunächst wurden die Proben in einem ersten ...
An intronic splice site alteration in combination with a large ...Semantic Scholar
www.semanticscholar.org
... Raimund Fahsold and Denise Horn and Luitgard Graul-Neumann}, journal={European journal of medical genetics}, year={2020}, pages={ }, url={https://api Raimund Fahsold and Denise Horn and Luitgard Graul-Neumann}, journal={European journal of medical genetics}, year={2020}, pages={ }, url={https://api ...
Attractions, Page Dresden, Germany, Public TransitMoovit
moovitapp.com
Raimund Fahsold FA F. Schulmuseum Dresden · Dr.Med. Hannelore Pigors · Wbs Finanzservice · Adva Berater · Congress Centre Dresden · Augustus Garten · Hotel ... Raimund Fahsold FA F. Schulmuseum Dresden · Dr.Med. Hannelore Pigors · Wbs Finanzservice · Adva Berater · Congress Centre Dresden · Augustus Garten · Hotel ...
Companies in Germany: D, 46Sales.Rocks
sales.rocks
Raimund Fahsold FA f. MolekularbiologieDr. Raimund Fussy ZahnarztDr. Raimund GeiselmannDr. Raimund HanischDr. Raimund KastDr. Raimund Kleine-HeringDr ... Raimund Fahsold FA f. MolekularbiologieDr. Raimund Fussy ZahnarztDr. Raimund GeiselmannDr. Raimund HanischDr. Raimund KastDr. Raimund Kleine-HeringDr ...
Dan-Christian Mentel - Manager-ProfilCompanyhouse
www.companyhouse.de
Netzwerk ; Martina Grohmann. 6 Verbindungen ; Peter Lorenz. 3 Verbindungen ; Raimund Fahsold. 1 Verbindung. Netzwerk ; Martina Grohmann. 6 Verbindungen ; Peter Lorenz. 3 Verbindungen ; Raimund Fahsold. 1 Verbindung.
Details zu: Untersuchungen zur molekularen Genetik der ...KIT - Karlsruher Institut für Technologie
katalog.bibliothek.kit.edu
Charakterisierung der nif Strukturgene / Raimund Fahsold. Von: Fahsold, Raimund [aut]. Resource type: Ressourcentyp: BuchBuchSprache: Deutsch Verlag: Charakterisierung der nif Strukturgene / Raimund Fahsold. Von: Fahsold, Raimund [aut]. Resource type: Ressourcentyp: BuchBuchSprache: Deutsch Verlag:
EVI2B, a Gene Lying in an Intron of the NeurofibromatosisMary Ann Liebert, Inc.
www.liebertpub.com
Raimund Fahsold, Christian Hein, Walther Vogel, Günter Assum Spinal Neurofibromatosis without. Café-au-Lait Macules in Two Families with Null ... Raimund Fahsold, Christian Hein, Walther Vogel, Günter Assum Spinal Neurofibromatosis without. Café-au-Lait Macules in Two Families with Null ...
Fatal glioblastoma multiforme in a patient with ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von F Distelmaier · · Zitiert von: 19 — Raimund Fahsold, Guido Reifenberger, Martina Messing-Juenger, Jörg Schaper, Dominik T Schneider, Ulrich Göbel, Ertan Mayatepek, Thorsten Rosenbaum ... von F Distelmaier · · Zitiert von: 19 — Raimund Fahsold, Guido Reifenberger, Martina Messing-Juenger, Jörg Schaper, Dominik T Schneider, Ulrich Göbel, Ertan Mayatepek, Thorsten Rosenbaum ...
HGQN - EinrichtungHGQN
www.hgqn.org
Raimund Fahsold. Ringversuchsleiter. Prof. Dr. Peter Steinbach. Abschlussbericht HD. molecular genetics. EMQN. M13 9WL Manchester. Vereinigtes ... Raimund Fahsold. Ringversuchsleiter. Prof. Dr. Peter Steinbach. Abschlussbericht HD. molecular genetics. EMQN. M13 9WL Manchester. Vereinigtes ...
Independent NF1 and PTPN11 mutations in a family with ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von C Thiel · · Zitiert von: 71 — Authors. Christian Thiel , Martin Wilken, Martin Zenker, Heinrich Sticht, Raimund Fahsold, Gabriele-Charlotte Gusek-Schneider, Anita Rauch ... von C Thiel · · Zitiert von: 71 — Authors. Christian Thiel , Martin Wilken, Martin Zenker, Heinrich Sticht, Raimund Fahsold, Gabriele-Charlotte Gusek-Schneider, Anita Rauch ...
Marfan syndrome with neonatal progeroid ...MedchemExpress.com
www.medchemexpress.com
Luitgard M Graul-Neumann 1, Tina Kienitz, Peter N Robinson, Sevjidmaa Baasanjav, Benjamin Karow, Gabriele Gillessen-Kaesbach, Raimund Fahsold, ... Luitgard M Graul-Neumann 1, Tina Kienitz, Peter N Robinson, Sevjidmaa Baasanjav, Benjamin Karow, Gabriele Gillessen-Kaesbach, Raimund Fahsold, ...
NF1 mutations in neurofibromatosis 1 patients with ...UKE
fis.uke.de
... Raimund Fahsold and Victor-F Mautner",. note = "Copyright Wiley-Liss, Inc.",. year = "2002",. month = mar,. day = "1",. doi = " humu.9018", Raimund Fahsold and Victor-F Mautner",. note = "Copyright Wiley-Liss, Inc.",. year = "2002",. month = mar,. day = "1",. doi = " humu.9018",.
Spinal neurofibromatosis without café-au-lait macules in ...Europe PMC
europepmc.org
von D Kaufmann · · Zitiert von: 61 — ... Raimund Fahsold,5 Christian Hein,4 Walther Vogel,1 and Günter Assum1. Dieter Kaufmann. Departments of 1Human Genetics, 2Dermatology, 3Neurology, and von D Kaufmann · · Zitiert von: 61 — ... Raimund Fahsold,5 Christian Hein,4 Walther Vogel,1 and Günter Assum1. Dieter Kaufmann. Departments of 1Human Genetics, 2Dermatology, 3Neurology, and
Udo Trautmann | Scholar Profiles and RankingsScholarGPS
scholargps.com
Raimund Fahsold (1). Renate Burger (1). Renate Kaulitz (1). Reza Asadollahi (1). Rolf Marschalek (1). Ronny Jung (1). Sabine Endele (1). Saleh Abdullah Al ... Raimund Fahsold (1). Renate Burger (1). Renate Kaulitz (1). Reza Asadollahi (1). Rolf Marschalek (1). Ronny Jung (1). Sabine Endele (1). Saleh Abdullah Al ...
Ulrike Hüffmeier上海情报服务平台
www.istis.sh.cn
Ulrike Hüffmeier Martin Zenker Juliane Hoyer Raimund Fahsold Anita Rauch · 《American Journal of Medical Genetics Part A》 · neurofibromatosis type 1 Noonan ... Ulrike Hüffmeier Martin Zenker Juliane Hoyer Raimund Fahsold Anita Rauch · 《American Journal of Medical Genetics Part A》 · neurofibromatosis type 1 Noonan ...
sortiert nach Relevanz / Datum