1
0
0
News
Biobanking Workshop and Symposium in Izmir - BBMRI-ERIC
www.bbmri-eric.eu
In the afternoon session, Rania Labib (Egypt), Imane Cherkaoui (Morocco), Maher Sughayer (Jordan), Ada Al-Qunaibet (Saudi Arabia), Sibel Ugur Iseri (Turkey) ... › news-events › biobanking-...
Network Profiles
LinkedIn: Ugur Iseri | LinkedIn
Ugur Iseri adlı kullanıcının LinkedIn'deki profesyonel profilini görüntüleyin. LinkedIn, Ugur Iseri gibi profesyonellere, tavsiye edilen iş adayları, sektör uzmanları ...
LinkedIn: Sibel A. Ugur Iseri - Associate Professor - Istanbul University | LinkedIn
En büyük profesyonel topluluk olan LinkedIn'de Sibel A. Ugur Iseri adlı kullanıcının profilini görüntüleyin. Sibel A. Ugur Iseri adlı kişinin profilinde 3 iş ilanı ...
Business Profiles
Just a moment...
www.zoominfo.com
View Sibel Ugur Iseri's business profile as Associate Professor at Istanbul University and see work history, affiliations and more.
Books & Literature
AbeBooks: : Locus and gene analyses in five inherited disorders:...
Locus and gene analyses in five inherited disorders: Genetic studies and statistical tools to analyze five inherited disorders in consanguineous families by...
Locus and gene analyses in five inherited disorders (Paperback)
www.loot.co.za
Ugur Iseri ; ; Genetics (non-medical), Life sciences: general ...
SIBEL UGUR ISERI - AbeBooks
www.abebooks.it
Locus and gene analyses in five inherited disorders di Ugur Iseri, Sibel e una vasta selezione di libri simili usati, antichi e fuori catalogo su AbeBooks.it.
bokus.com: Sibel Ugur Iseri - Böcker | Bokus bokhandel
Köp böcker av Sibel Ugur Iseri:
Music
Sibel Ugur Iseri · Locus and Gene Analyses in Five Inherited ...igames.dk › Books › Sibel Ugur Iseri
imusic.dk
Genetic analyses in five inherited disorders In this study, computer based parametric tests including two and multi point analysis and simulation were applied to ...
Related Documents
Digitala Vetenskapliga Arkivet - DiVA
www.diva-portal.org
by Y Yıldırım · · Cited by 55 — Digitala Vetenskapliga Arkivet · Yıldırım, Yeşerin · Kocasoy Orhan, Elif · Ugur Iseri, Sibel Aylin · Serdaroglu-Oflazer, Piraye · Kara, Bülent ... › smash › record
GUCY2D gene - MedlinePlus
medlineplus.gov
Aug 18, — Ugur Iseri SA, Durlu YK, Tolun A. A novel recessive GUCY2D mutation causingcone-rod dystrophy and not Leber's congenital amaurosis. › download › genetics › g...
EBSCOhost | | Use of genome-wide SNP homozygosity mapping in...
web.b.ebscohost.com
Sibel Ugur Iseri • Alexander W. Wyatt • Gudrun Nürnberg •. Christian Kluck • Peter Nürnberg • Graham E. Holder •. Ed Blair • Alison Salt • Nicola ...
frameshift mutation of ERLIN2 in recessive intellectual ...
academic.oup.com
by Y Yıldırım · · Cited by 55 — Sibel Aylin Ugur Iseri,. Sibel Aylin Ugur Iseri. 1. Department of Molecular Biology and Genetics. ,. Boğaziçi University. ,. Istanbul › hmg › article-abstract
Scientific Publications
A clinical variant in SCN1A inherited from a mosaic father ...
www.sciencedirect.com
... UzunMahmut S.SagirogluBetulYuceturkBayramYukselBetulBaykanNersesBebekAkinIscanSibel A.Ugur Iseri UgurOzbek. Show more.
A novel recessive GUCY2D mutation causing cone-rod dystrophy and not...
pubmed.ncbi.nlm.nih.gov
PubMed comprises more than 30 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to...
Bunyan DJ[au] - Search Results - PubMed
www.ncbi.nlm.nih.gov
Bunyan DJ[au] - Search Results - PubMed
Characterization of the C. elegans erlin homologue | BMC Molecular...
bmcmolcellbiol.biomedcentral.com
Yildirim Y, Kocasoy Orhan E, Ugur Iseri SA, Serdaroglu-Oflazer P, Kara B, Solakoglu S, Tolun A: A frameshift mutation of ERLIN2 in recessive intellectual disability
Publications
PANOGA identifies the neurotrophin pathway using the genome-wide DNA...
core.ac.uk
By Ozkan Ozdemir ( ), Ece Egemen ( ), Sibel Aylin Ugur Iseri ( ), Osman Ugur Sezerman ( ), Nerses Bebek ( ), Betul ...
Identification and functional characterisation of genetic variants in...
link.springer.com
Anophthalmia, microphthalmia, and coloboma are a genetically heterogeneous spectrum of developmental eye disorders and affect around 30 per 100,000 live bi
Sibel Aylin Ugur - Wikidata
www.wikidata.org
Sibel Ugur; Sibel Ugur Iseri. In more languages. Spanish. Sibel Aylin Ugur. No description defined. Traditional Chinese. No label defined. › wiki
Video & Audio
BOĞAZİÇİ ÜNİVERSİTESİ - Doç. Dr. Sibel Uğur İşeri - Moleküler...
www.universitetercihleri.com
BOĞAZİÇİ ÜNİVERSİTESİ - Doç. Dr. Sibel Uğur İşeri - Moleküler Biyoloji ve Genetik Bölümü Mezunu | Üniversite Tercihleri
Reports & Statements
Books by author - sibel ugur iseri (1) - Rediff.com -Booksbooks.rediff.com › author › sibel-ugur-iseri
books.rediff.com
Buy Sibel Ugur Iseri books in India. Collection of books by Sibel Ugur Iseri : Locus and Gene Analyses in Five Inherited Disorders available at Rediff Shopping.
Locus and Gene Analyses in Five Inherited Disorders | Book by ...books.rediff.com › Genetics (non-medical)
books.rediff.com
Locus and Gene Analyses in Five Inherited Disorders by Sibel Ugur Iseri. Buy Locus and Gene Analyses in Five Inherited Disorders online for Rs. (4304) - Free ...
Miscellaneous
Sibel A. Ugur Iseri | LinkedIn
www.linkedin.com
View Sibel A. Ugur Iseri's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Sibel A. Ugur Iseri discover ...
Ugur Iseri | LinkedIn
www.linkedin.com
View Ugur Iseri's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Ugur Iseri discover inside ...
Piraye Oflazer - Google Scholar Citationsscholar.google.com/citations?user=cgzpeBEAAAAJ&hl=en
scholar.google.com
A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures. Y Yıldırım, E Kocasoy Orhan, SA Ugur Iseri, ...
Libro locus and gene analyses in five inherited disorders, ugur iseri ...
www.buscalibre.cl
Libro locus and gene analyses in five inherited disorders, ugur iseri, sibel, ISBN Comprar en Buscalibre - ver opiniones y comentarios.
Locus and gene analyses in five inherited disorders - Sibel Ugur Iseri
www.payot.ch
› Detail › locus...
Meaning of baby name Ugur iseri in different languages
namesof.com
Meaning of baby name Ugur iseri in different languages
ugur iseri | SchoolBANK.nl - vind je oude klasgenoten terug
www.schoolbank.nl
Stuur een bericht naar ugur iseri. Je hebt al een gesprek met ugur iseri. Kies of je die wil voortzetten, of selecteer 'nieuw' als je een nieuw gesprek wil starten.
Locus and gene analyses in five inherited disorders - Ugur Iseri,...
www.prospero.hu
Locus and gene analyses in five inherited disorders, Ugur Iseri, Sibel; : , 108 pages; Genetic analyses in five inherited disorders In this study, computer...
Ugur iseri | Meaning Pronunciation Origin of Baby Name Ugur iseri frm...
namesof.com
Ugur iseri : Baby Name Ugur iseri Meaning,Pronunciation,Origin,Religion,Pronounce of Baby Name Ugur iseri. Similar Names ,All about the name Ugur iseri Are you...
Résultats de la recherche pour " Sibel Ugur Iseri"
www.morebooks.de
Locus and gene analyses in five inherited disorders. Genetic studies and statistical tools to analyze five inherited disorders in consanguineous families.
DEFINE_ME
www.brainanddevelopment.com
A novel gene mutation in PANK2 in a patient with severe jaw-opening dystonia. Zuhal Yapici. x Sibel Aylin Ugur Iseri.
A Novel GUCY2D Mutation, V933A, Causes Central Areolar Choroidal...
iovs.arvojournals.org
Ugur Iseri SA, Durlu YK, Tolun A. A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis. Eur J Hum Genet .
Molecular Vision: A novel GUCY2D mutation in a Chinese family with...
www.molvis.org
2009; 125:349 [PMID: ]; Ugur Iseri SA, Durlu YK, Tolun A. A novel recessive GUCY2D mutation causing cone-rod dystrophy and not ...
GUCY2D gene - Genetics Home Reference - NIH
medlineplus.gov
The GUCY2D protein is involved in a chemical reaction that helps return photoreceptors to their dark state after light exposure Ugur Iseri SA, Durlu YK, Tolun A.
OMIM Entry # CONE-ROD DYSTROPHY 6; CORD6
omim.org
CONE-ROD DYSTROPHY 6; CORD RETINAL CONE DYSTROPHY 2; RCD
A novel gene mutation in PANK2 in a patient with severe jaw ...
www.brainanddevelopment.com
Zuhal Yapici, Nihan Hande Akcakaya, Pinar Tekturk, Sibel Aylin Ugur Iseri, Ugur Ozbek. Brain and Development. Volume 38 Issue 8 Pages (September ... › article › ppt
Related search requests for Ugur Iseri
| Ozkan Ozdemir Ugur Ozbek Betul Baykan | Ugur Sezerman Osman Ugur Aylin Ugur |
People Forename "Ugur" (1727) Name "Iseri" (161) |
sorted by relevance / date