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News
The Phenotype Of Second And Third Toe Syndactyly Maps To Chromosome...
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Telephone & Addresses
Frank A Oeffner, Vero Beach, US, Heritage Blvd
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Last Name: Oeffner (Page 1) - Advanced Background Checks
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Evelyn Oeffner · Florence Oeffner · Frances Oeffner · Francis Oeffner · Frank Oeffner · Frederick Oeffner · Fredk Oeffner · Gary Oeffner · Gayle Oeffner · Gerard ...
Network Profiles
LinkedIn: Frank Oeffner | LinkedIn
View Frank Oeffner’s profile on LinkedIn, the world's largest professional community. Frank has 2 jobs listed on their profile. See the complete profile on LinkedIn ...
LinkedIn: Frank Oeffner | LinkedIn
Frank Oeffners berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Frank Oeffner dabei hilft, ...
Interests
Lisch corneal dystrophy is genetically distinct from Meesmann corneal...
www.em-consulte.com
Walter Lisch, MD ⁎ , Andreas Büttner, MD, Frank Oeffner, PhD, Inke Böddeker, Hartmut Engel, Christina Lisch, MD, Andreas Ziegler, PhD, Karl-Heinz Grzeschik, ...
American Journal of Opthalmology - Vol n° 4 - EM consulte
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American Journal of Opthalmology - Présentation - EM consulte
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Walter Lisch, MD a * , Andreas Büttner, MD b, Frank Oeffner, PhD ... Lisch corneal dystrophy is genetically different from Meesmann corneal dystrophy.
Business Profiles
Employees
Team – Dr. rer. physiol. Frank Oeffner – genetikum
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Dr. rer. physiol. Frank Oeffner, Fachhumangenetiker, DNA-Diagnostik
Heritage
Frank Oeffner in the Census | Ancestry®
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View Frank Oeffner's US census record to find family members, occupation details & more. Access is free so discover Frank Oeffner's story today.
Oeffner - Ancestry.co.uk
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Name: Frank Oeffner. Birth: year. Departure: location. Arrival: date - New York, New York. New York, Passenger Lists, Immigration & Travel
Oeffner - New York, Passenger Lists, Ancestry.co.uk
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Frank Oeffner, date, year, location, race, ship name. View Record. Wilhelm Oeffner, date, year, location, race, ship name. View Record. Louise Oeffner, date ...
Books & Literature
Books by frank oeffner - Biblio.com
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Frank Oeffner | XanEdu Customization Platform
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Author: Frank Oeffner. Results. Is the risk of multiple sclerosis related to the 'biography' of the immune system? Springer Science+Business Media
Molekularmedizinische Grundlagen von Endokrinopathien - Google Books
books.google.de
... Dr. FRANK OEFFNER Philipps-Universität Marburg Institut für Humangenetik , Marburg e-mail: ...
Analyse der funktionellen Epitope des Glykoproteins...
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Save on ISBN Biblio.co.uk has Analyse der funktionellen Epitope des Glykoproteins HEF der Influenza-C-Viren mit molekularbiologischen Methoden...
Related Documents
CiteSeerX — Zentrum für Humangenetik,
citeseerx.ist.psu.edu
BibTeX @MISC{Oeffner_zentrumfür, author = {Frank Oeffner and Christine Schäfer and Barbara Fritz and Aurelia Lara Fuchs and Rainer König and Marburg Deutschland}, ...
A Novel Type of Autosomal Recessive Syndactyly | Hand | Polymerase...
de.scribd.com
A Novel Type of Autosomal Recessive Syndactyly: ... Sajid Malik,1,2* Muhammad Arshad,2 Muhammad Amin-ud-Din,3 Frank Oeffner,1 Astrid Dempfle,4
Menkes disease with discordant phenotype in female monozygotic twins,...
www.deepdyve.com
CLINICAL REPORT. Menkes Disease with Discordant Phenotype in. Female Monozygotic Twins. Anna Lena Burgemeister,. 1. * Birgit Zirn,. 1,2. Frank Oeffner,. 1.
PORCN mutations in focal dermal hypoplasia: coping with lethality
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www.hgvs.org. PORCN Mutations in Focal Dermal Hypoplasia: Coping with Lethality. Dorothea Bornholdt. 1. , Frank Oeffner. 1. , Arne König. 2.
Scientific Publications
Dr. Frank Oeffner - Gepris - DFG
gepris.dfg.de
Dr. Frank Oeffner. Als Antragsteller abgeschlossene Projekte. Bardet-Biedl- Syndrom 4: Molekulare Analyse eines pleiotropen Genlocus (Sachbeihilfe).
AJO | American Journal of Ophthalmology | Vol 130, Issue 4, Pages...
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Walter Lisch, Andreas Büttner, Frank Oeffner, Inke Böddeker, Hartmut Engel, Christina Lisch, Andreas Ziegler, Karl-Heinz Grzeschik; Abstract PDF (643 K)
Verfasser Suchresultate
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Treffer von 16 für Suche: 'Frank Oeffner'. Sortieren. Relevanz, Erscheinungsjahr, absteigend, Erscheinungsjahr, aufsteigend, Person / Institution, Titel ...
Forschung mit Gänsehaut-Faktor: Humangenetiker finden Gen des...
www.bionity.com
Genetische Tippfehler mit haarigen Folgen: Marburger Mediziner haben die Ursache des so genannten IFAP-Syndroms gefunden, einer seltenen Erbkrankheit, die bei...
Publications
Oeffner, Frank [WorldCat Identities]
orlabs.oclc.org
Analyse der funktionellen Epitope des Glykoproteins HEF der Influenza-C-Viren mit molekularbiologischen Methoden by Frank Oeffner ( Book ) 2 editions ...
Publications Authored by Frank Oeffner | PubFacts
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Publications Authored by Frank Oeffner
Is the risk of multiple sclerosis related to the ‘biography’ of the...
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Is the risk of multiple sclerosis related to the ‘biography’ of the ... Frank Oeffner, John M ... Is the risk of multiple sclerosis related to the ‘biography ...
Frank Oeffner's Research | CureHunter
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Frank Oeffner Selected Research. Frank Oeffner Research Ichthyosis (Xeroderma) Photophobia (Light Sensitivity)
Reports & Statements
Wikipedia: Podoplanina – Wikipedia, wolna encyklopedia
Skocz do góry ↑ Gert Zimmer, Frank Oeffner, V. V. Messling, Thomas Tschernig i inni. Cloning and characterization of gp36, a human mucin-type glycoprotein ...
Deficiency of PORCN, a regulator of Wnt signaling, is associated with...
www.nature.com
Brief Communication
Miscellaneous
Frank Oeffner | LinkedIn
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View Frank Oeffner's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Frank Oeffner discover inside ...
Öffnungszeiten - Dr. Frank Oeffner, Neu,
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Öffnungszeiten von Dr. Frank OeffnerNeu. Arzt offen von Montag bis Freitag.
Dr. Frank Oeffner in Neu-Ulm - Humangenetik
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Dr. Frank Oeffner, in Neu-Ulm. Fachgebiete: Humangenetik
Frank Oeffner | Philipps University Marburg - Academia.edu
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GMS | GMS Journal for Medical Education | Interactive e-learning...
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Authors Frank Oeffner - Philipps-Universität Marburg, Zentrum für Humangenetik, Marburg, Deutschland Christine Schäfer - Philipps-Universität Marburg ...
(PDF) IFAP Syndrome Is Caused by Deficiency in MBTPS2, an...
www.academia.edu
Frank Oeffner. Karl-Heinz Grzeschik. Rudolf Happle. Silke Redler. Dorothea Bornholdt. Ulrike Neidel. connect to download. Get pdf. IFAP Syndrome Is Caused by ...
(PDF) Lisch corneal dystrophy is genetically distinct from Meesmann...
www.academia.edu
Frank Oeffner. Karl-Heinz Grzeschik. connect to download. Get pdf. Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3.
Altmetric – Multiple familial trichoepithelioma caused by mutations...
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Authors. Aicha Salhi, Dorothea Bornholdt, Frank Oeffner, Sajid Malik, Ernest Heid, Rudolf Happle, Karl-Heinz Grzeschik. Abstract. The recessive oncogene ...
American Journal of Ophthalmology - Related By Results
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Walter Lisch, Andreas Büttner, Frank Oeffner, Inke Böddeker, Hartmut Engel, Christina Lisch, Andreas Ziegler, Karl-Heinz Grzeschik et al. Full-length article
Deficiency of PORCN, a regulator of Wnt signaling, is associated with...
moh-it.pure.elsevier.com
Karl Heinz Grzeschik ; Dorothea Bornholdt ; Frank Oeffner ; Arne König ; María Del Carmen Boente ; Herbert Enders ; Barbara Fritz ; Michael Hertl ; Ute ...
IFAP Syndrome Is Caused by Deficiency in MBTPS2, an Intramembrane...
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Frank Oeffner, Gayle Fischer, Rudolf Happle, Arne König, Regina C. Betz, Dorothea Bornholdt, Ulrike Neidel, María del Carmen Boente, Silke Redler, Javier ...
Kommissionen des BVDH e.V. | BVDH
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PD Dr. rer. physiol. Frank Oeffner, Neu-Ulm. Kommission Qualitätssicherung. Mitglieder der Kommission Prof. Dr. rer. nat. Jürgen Kunz, Berlin (Sprecher) Prof.
Lisch corneal dystrophy is genetically distinct from Meesmann corneal...
www.infona.pl
Frank Oeffner. Institute of Human Genetics of the University of Marburg (Dr Oeffner, Mr Engel, and Dr Grzeschik), Marburg, Germany. autor. Inke Böddeker.
Menkes disease with discordant phenotype in female monozygotic twins -
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Authors: Anna Lena Burgemeister, Birgit Zirn, Frank Oeffner, Stephen G. Kaler, Gunther Lemm, Eva Rossier, Hans‐Martin Büttel. Journal ...
MBTPS2
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Research Grants, Species, Publications, Scientific Experts, Genomes and Genes, Research Topics about MBTPS2
Scilit | Article - Menkes disease with discordant phenotype in female...
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Menkes disease with discordant phenotype in female monozygotic twins. Anna Lena Burgemeister, Birgit Zirn, Frank Oeffner, Stephen G. Kaler, ...
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