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LinkedIn: Mohsen Karbasiyan – Dipl.-Ing – Charité | LinkedIn
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LinkedIn: Mohsen Karbasiyan | LinkedIn
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Business Profiles
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Researchgate: Mohsen Karbasiyan
Berlin, Germany
Private Homepages
mehrabaseman.com - bgp.he.netbgp.he.net › dns › mehrabaseman
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... mohsen karbasiyan Registrant Organization: None Registrant Street: tehran Registrant City: null Registrant State/Province: null Registrant Postal Code:
Books & Literature
PLOS Genetics: Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New...
journals.plos.org
PLOS Genetics is an open-access
The Slavic NBN Founder Mutation: A Role for PLOS ONE
journals.plos.org
Véronique Dutrannoy. Affiliation Institute of Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Germany. Mohsen Karbasiyan.
Related Documents
CiteSeerX — M: Fatal cardiac arrhythmia and long-QT syndrome in a new...
citeseerx.ist.psu.edu
... and Dominik Seelow and Raymonda Varon and Rita Barresi and Anne Schulze and Barbara Lucke and Susanne Lützkendorf and Mohsen Karbasiyan and Sebastian ...
Epigenetic Clock and Relative Telomere Length Represent Largely...
academic.oup.com
Mohsen Karbasiyan. Institute of Medical and Human Genetics, Charité- Universitätsmedizin Berlin, Germany. Search for other works by this ...
Allelic heterogeneity in the COH1 gene explains clinical variability...
www.scienceopen.com
Authors: Jake T. Neumann, Sameer Al-Harthy, Elisabeth Moser, Hans Hennies, Katja M Eckl, Mohsen Karbasiyan, Małgorzata Krajewska, ...
EBSCOhost | | Fcγ-Receptor IIIA Polymorphism p.158F Has No...
web.b.ebscohost.com
Petra Reinke,4 Ruth Neuhaus,5 Mohsen Karbasiyan,6 Barbara Gärtner,7. Ioannis Anagnostopoulos,8 Hanno Riess,2 Ralf U. Trappe,1,2 and ...
Scientific Publications
FragIdent – Automatic identification and characterisation of...
bmcgenomics.biomedcentral.com
Many genetic studies and functional assays are based on cDNA fragments. After the generation of cDNA fragments from an mRNA sample, their content is at first...
Mohsen Karbasiyan – ScienceOpen
www.scienceopen.com
Cohen syndrome is a rare autosomal recessive disorder with a variable clinical picture mainly characterized by developmental delay, mental retardation, ...
Publications
FCY-receptor IIIA polymorphism p.158F has no negative predictive...
core.ac.uk
By Heiner Zimmermann, Theresa Weiland, Jamie P. Nourse, Maher K. Gandhi, Petra Reinke, Ruth Neuhaus, Mohsen Karbasiyan, Barbara Gärtner, Ioannis ...
Fcγ-Receptor IIIA Polymorphism p.158F Has No …
www.hindawi.com
We retrospectively analyzed the p.V158F polymorphism of Fc; Ruth Neuhaus, and Hanno Riess recruited the patients. Theresa Weiland, Mohsen Karbasiyan, ...
Identification of a novel candidate gene for non-syndromic ...www.wikidata.org › wiki
www.wikidata.org
1 reference. stated in · Europe PubMed Central · PubMed ID · · retrieved. 13 September Mohsen Karbasiyan. series ordinal. 5.
Video & Audio
YouTube
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Reports & Statements
cardiodreamteam.com • Просмотр темы - Синдром удлиненного QT
cardiodreamteam.com
... Barresi, Anne Schulze, Barbara Lucke, Susanne Lützkendorf, Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke
Spectrum of mutations and genotype–phenotype analysis in Currarino...
www.nature.com
The triad of a presacral tumour, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by dorsal-ventral patterning...
Spectrum of mutations and genotype–phenotype Nature
www.nature.com
Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome. Joachim Köchling ,; Mohsen Karbasiyan &; André Reis.
Miscellaneous
Allelic Heterogeneity in the COH1 Gene SlidePlayerslideplayer.com › slide
slideplayer.com
... Roberto Giugliani, Thomas E. Neumann, Katja M. Eckl, Mohsen Karbasiyan, André Reis, Denise Horn The American Journal of Human Genetics Volume 75, ...
Reverse Whois | Domain Ownership Search | DomainTools
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Find every domain name ever owned by any individual or company with Reverse Whois. Find current and/or historical Whois records and build an ownership profile.
Mr Mohsen KARBASIYAN - Orphanetwww.orpha.net › cgi-bin › Directory_Professionals › MIS...
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Mr Mohsen KARBASIYAN. Activities registered with Orphanet : Quality manager; E-mail : email; Phone : 49 (0) ; Mobile : -. Labor Berlin - Charité ...
Mohsen Karbasiyan: free download. Ebooks library. On-line books store...
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Mohsen Karbasiyan: free download. Ebooks library. On-line books store on Z-Library | BookSC. Download books for free. Find books
Mr Mohsen KARBASIYAN - Orphanet
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Labor Berlin - Charité Vivantes GmbH - Fachbereich Humangenetik; Institut für Medizinische Genetik und Humangenetik; Charité - Universitätsmedizin Berlin ...
Allelic Heterogeneity in the COH1 Gene Explains Clinical Variability...
pure.hud.ac.uk
... Malgorzata Krajewska-Walasek, Anna Rajab, Roberto Giugliani, Thomas E. Neumann, Katja M. Eckl, Mohsen Karbasiyan, André Reis, Denise Horn.
Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of...
journals.plos.org
Mohsen Karbasiyan, Affiliation: Institute of Human Genetics, Charité University Medical School, Berlin, Germany ⨯ Sebastian Bachmann, Affiliations ...
Epigenetic Clock and Relative Telomere Length X-MOLwww.x-mol.com › paper
en.x-mol.com
Valentin Max Vetter, Antje Meyer, Mohsen Karbasiyan, Elisabeth Steinhagen- Thiessen, Werner Hopfenmüller, Ilja Demuth. DNA methylation ...
Allelic Heterogeneity in the COH1 Gene Explains Clinical...
www.infona.pl
Cohen syndrome is a rare autosomal recessive disorder with a variable clinical picture mainly characterized by developmental delay, mental retardation,...
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural ...
scite.ai
... Rumaisa Bashir, Elizabeth Vafiadaki, Silva Ivanova, Thomas Raffelsberger, Isabel Maerk, Harald Höger, Martin Jung, Mohsen Karbasiyan, Maria Storch, Hans ...
Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New ...figshare.com › articles › Fatal_Cardiac_Arrhythmia_and_...
figshare.com
... Rita Barresi Anne Schulze Barbara Lucke Susanne Lützkendorf Mohsen Karbasiyan Sebastian Bachmann Simone Spuler Markus Schuelke.
Volume 02 Issue 11 November 2014
jmscr.igmpublication.org
Authors: Reham Moftah, Raymonda Varon, Christiane Bommer, Véronique Dutrannoy, Mohsen Karbasiyan, Salah Marzouk, Dalal El-Kaffash, ...
Identifikation und Charakterisierung des Gens für das Cohen-Syndrom
forschungsberichte.charite.de
Dr.med. Denise Horn
Heterozygous carriers of germline c.657_661del5 founder ...read.qxmd.com › read
read.qxmd.com
... Igor Resnick, Ivo Kremensky, Kathrin Saar, Katrin Hoffmann, Véronique Dutrannoy, Mohsen Karbasiyan, Mehdi Ghani, Ivo Barić, Mustafa Tekin, Peter Kovacs, ...
Most recent papers with the keyword Epigenetic clock | Read ...
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Valentin Max Vetter, Meyer Antje, Mohsen Karbasiyan, Elisabeth Steinhagen-Thiessen, Werner Hopfenmüller, Ilja Demuth. DNA methylation age (DNAm age; ...
Farmanmusic.com - Farm An Music - WHOIS & Domain Review
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Farmanmusic.com is owned by Mohsen Karbasiyan. Farmanmusic.com Whois Record, Domain History, Name Servers, IP, Geolocation
PLOS Genetics: Publishing science, accelerating research
journals.plos.org
... , Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke PLOS Genetics: published 12 Mar ...
Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of ...
figshare.com
Liza J. McCann. Dominik Seelow. Raymonda Varon. Rita Barresi. Anne Schulze. Barbara Lucke. Susanne Lützkendorf. Mohsen Karbasiyan.
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