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Images of Hermann-Josef Lüdecke
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Essener Forscher identifizieren Ursache des Burn-McKeown-Syndroms:...
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Hermann-Josef Lüdecke vom Institut für Humangenetik der Medizinischen Fakultät der Universität Duisburg Essen am Universitätsklinikum ...
Medizinische Fakultät News
www.uni-due.de
News und Aktuelles aus der Forschung Medizinischen Fakultät der Universität Duisburg-Essen und des Universitätsklinikums Essen
Network Profiles
LinkedIn: Hermann-Josef Lüdecke | LinkedIn
Hermann-Josef Lüdeckes berufliches Profil anzeigen LinkedIn ist das weltweit größte professionelle Netzwerk, das Fach- und Führungskräften wie Hermann-Josef ...
Personensuche
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Dr. rer. nat. Hermann-Josef Lüdecke · KONTAKT · IMPRESSUM · Datenschutz. Letzte Änderung: | © Universität Duisburg-Essen webmaster@uni-due.
Employees
Marcel Martin — Lehrstuhl 11 Algorithm Engineering
ls11-www.cs.tu-dortmund.de
Marcel Martin, Sven Rahmann Christopher Teller, Marcel Martin, Sven Rahmann, Ute Hehr, Han G Brunner, Hermann-Josef Lüdecke and Dagmar Wieczorek. ...
Books & Literature
Oto-facial syndrome and esophageal atresia, intellectual disability...
biblio.ugent.be
... Christopher Teller, Marcel Martin, Sven Rahmann, Ute Hehr, Han G Brunner, Hermann-Josef Lüdecke and Dagmar Wieczorek; organization.
- مقالات نوشته شده توسط Hermann-Josef Lüdecke سایپرز، باشگاه
www.scipers.com
Rheumatologic and neurological events in an elderly patient with tricho-rhino- phalangeal syndrome type I سال انتشار: July–August ژورنال: European ...
Epstein's Inborn Errors of Development: The Molecular Basis of...
books.google.de
This third edition of Epstein's Inborn Errors of Development provides essays on pathways of development and thoughtful reviews of dysmorphic syndromes for...
Prader-Willi Syndrome: and Other Chromosome 15q Deletion Disorders -...
books.google.de
Although Prader-Willi syndrome was first described 35 years ago, it was following detection of an interstitial chromosome 15q deletion in some affected...
Related Documents
Hermann-josef Lüdecke - Academia.edu
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Expression of Trps1 during mouse embryonic development – ScienceOpen
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Expression of Trps1 during mouse embryonic development. Authors: Andrea Vortkamp, Melanie Kunath, Hermann-Josef Lüdecke. Publication ...
Oto-facial syndrome and esophageal atresia, intellectual disability...
www.scienceopen.com
Bernd Schweiger. Marloes Steehouwer. Christopher Teller. Marcel Martin. Sven Rahmann. Ute Hehr. Han G Brunner. Hermann-Josef Lüdecke.
Scientific Publications
Dr. Hermann-Josef Lüdecke - Gepris - DFG
gepris.dfg.de
Dr. Hermann-Josef Lüdecke. Als Antragsteller abgeschlossene Projekte. Funktionelle Analyse des TRPS1 Zinkfinger-Proteins und seine Rolle in der ...
Genomic Organization and Promoter Structure of the Human EXT1 Gene -...
www.sciencedirect.com
Hermann-Josef Lüdecke a; Jung Ahn b; X. Lin b; A. Hill b; Michael J. Wagner b, 11Present address: Glaxo Wellcome, Five Moore Drive, Research Triangle Park, ...
A position effect on TRPS1 is associated with Ambras syndrome in...
www.ncbi.nlm.nih.gov
We thank Dr Hermann-Josef Lüdecke for the marker TAGA and for stimulating discussions.
DuEPublico: Person Dr. Lüdecke, Hermann-Josef
duepublico.uni-duisburg-essen.de
· KONTAKT · IMPRESSUM. © Universität Duisburg-Essen | - - due.de.
Publications
Two RFLPs at the D8S50 locus - CORE
core.ac.uk
By Bernhard Horsthemke, Ruth Burdiek and Hermann-Josef Lüdecke. Abstract. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid= Topics: http ...
Publications Authored by Alma Kuechler | PubFacts
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Publications Authored by Alma Kuechler
Construction and characterization of band-specific DNA libraries |...
link.springer.com
A universally primed polymerase chain reaction was developed to amplify DNA dissected from GTG-banded human chromosomes. The amplification products are clo
Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and...
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PubFacts seeks to make the world's scientific research easy to locate, access, and collaborate on.
Reports & Statements
Kliniken - u.a. Unfall-Chirurgie; Uni-Kliniken, Humangenetik -...
orpha-selbsthilfe.de
Kliniken - u.a. Unfall-Chirurgie; Uni-Kliniken, Humangenetik - Anschriften
Miscellaneous
Hermann-Josef Lüdecke | LinkedIn
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Hermann-Josef Lüdecke. Scientist bei Universitaetsklinikum Standort Köln und Umgebung, Deutschland Branche Medical Practice
Hermann-Josef Lüdecke - Scientist - Universitaetsklinikum ...
www.linkedin.com
View Hermann-Josef Lüdecke’s profile on LinkedIn, the world's largest professional community. Hermann-Josef has 1 job listed on their profile. See the complete profile on LinkedIn and discover ...
TRPS & MHE - Yahoo! Groups
de.groups.yahoo.com
Diese von Dr. Hermann-Josef Lüdecke ins Leben gerufene Gruppe verfolgt das Ziel, das Wissen zu den TRP-Syndromen sowie zu MHE zu vermehren und zu ...
(PDF) Three RFLPs at the D8S49 locus | Hermann-josef Lüdecke -...
www.academia.edu
Three RFLPs at the D8S49 locus
Hermann-Josef Lüdecke
www.infona.pl
Melanie Kunath, Hermann-Josef Lüdecke, Andrea Vortkamp · Mechanisms of Development 119 , Supplement , S117-S120. The Trps1 ...
LIVIVO - Search results - AU="Lüdecke, Hermann-Josef"
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(PDF) Expression of Trps1 during mouse embryonic development |...
www.academia.edu
Hermann-josef Lüdecke. Andrea Vortkamp. Download with Google Download with Facebook or download with email. Expression of Trps1 during mouse embryonic development. Download. Expression of Trps1 during mouse embryonic development. Authors. H. Lüdecke + 1. Hermann-josef Lüdecke. Andrea Vortkamp.
(PDF) RAD21 Mutations Cause a Human Cohesinopathy | Hermann-josef...
www.academia.edu
Hermann-josef Lüdecke. Frank Kaiser. Matthew Deardorff. S. Spranger. Download with Google Download with Facebook or download with email. RAD21 Mutations Cause a Human Cohesinopathy. Download. RAD21 Mutations Cause a Human Cohesinopathy. Authors. H. Lüdecke + 3. Hermann-josef Lüdecke. Frank Kaiser.
Genmutationen als Ursache für p3-Syndrom
medonline.at
Ein Wissenschafter-Team mit österreichischer Beteiligung entdeckte, dass Mutationen des Setd5-Gens für das
A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations...
www.zora.uzh.ch
... Karin Buiting, Claudia Dufke, Encarna Guillén-Navarro, Diana S Johnson, Udo Koehler, Vanesa López-González, Hermann-Josef Lüdecke, ...
All transcript variants in gene CPLX1 - Global Variome shared LOVD
databases.lovd.nl
(Cys105*), g G>T, g G>T, -, -, CPLX1_ , -, Redler S et al, submitted, -, -, Germline, yes, -, -, 0, -, Hermann-Josef Lüdecke. +?/. 4 · c.315C>A ...
Congenital/Metabolic
www.thedoctorsdoctor.com
... Hermann-Josef Lüdecke, PhD; Nicola Wagner, MD; Eva-Bettina Bröcker, MD; Henning Hamm, MD . Arch Dermatol ;137: Abstract quote ...
De Novo and inherited loss-of-function variants in TLK2: Clinical and...
eprints.soton.ac.uk
Author: Hermann-Josef Lüdecke. Author: Jacqueline Eason. Author: Gijs W.E. Santen. Author: Jill Clayton-Smith. Author: Kate Chandler. Author: Katrina Tatton- ...
Hypochondroplasie / TRPS / MHE Eltern- und Betroffenenseminar ...
mx.eventbu.com
... von Dr. Joachim Lauen von der Berufsgenossenschaftlichen Unfallklinik Murnau, Dr. Hermann-Josef Lüdecke von der Universitätsklinik Düsseldorf und Prof.
November 1, Issue of JAMA Dermatology | JAMA Network
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Read the November 1, issue. Volume 137, Number 11
OPUS FAU | A new face of Borjeson–Forssman–Lehmann syndrome? De novo...
opus4.kobv.de
... André Reis, Bernd Wollnik, Michael Zeschnigk, Hermann-Josef Lüdecke, Dagmar Wieczorek. Background: Borjeson–Forssman–Lehmann ...
مقاله جهش در ژن EXT1 و EXT2 در اگزوستوز متعدد ارثی - سایپرز
www.scipers.com
... Genetics () توسط Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, Florindo Mollica, Hermann-Josef Lüdecke, ...
RAD21 Mutations Cause a Human Cohesinopathy
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Hermann-Josef Lüdecke. Institut für Humangenetik, Universität Duisburg Essen, Essen , Germany. autor. Robert G. Ramsay. Research Division, Peter ...
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