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Decreased subfoveal choroidal thickness and failure of...
bjo.bmj.com
Levent Karabas,1 Fehim Esen,2 Hande Celiker,2 Nursel Elcioglu,3 Eren Cerman ,2. Muhsin Eraslan,2 Haluk Kazokoglu,2 Ozlem Sahin2.
Business-Profile
Nursel H Elçioglu Marmara UniversityResearchGate
www.researchgate.net
Purpose: To investigate the molecular basis of recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and ...
Ausbildung
Human MutationScholars Portal Journals
journals.scholarsportal.info
Carla Martins · Paula Frassinetti V. Medeiros · Sandra Leistner‐Segal · Larbi Dridi · Nursel Elcioglu · Jill Wood · Mahdiyeh Behnam · Bilge Noyan ...
Bücher
Ptosis as a unique hallmark for autosomal recessive WNT1-associated...
biblio.ugent.be
Nampoothiri, Sheela, Brecht Guillemyn, Nursel Elcioglu, Sujatha Jagadeesh, Dhanya Yesodharan, Beena Suresh, Serap Turan, Sofie ...
JIMD Reports, Volume Google Books
books.google.de
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously...
JIMD Reports, Volume Seite 8 - Google Books-Ergebnisseitegoogle.com
books.google.com
Alessandra Zanetti, Neslihan Önenli-Mungan, Nursel Elcioglu, Mehmet Nuri Özbek, Deniz K€or, Elisabetta Lenzini, and Rosella Tomanin declare no conflicts of ...
Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic...
journals.plos.org
PLOS Genetics is an open-access
Dokumente zum Namen
Colobomatous macrophthalmia with microcornea syndromeWiley Online Library
onlinelibrary.wiley.com
von E Toker · · Zitiert von: 29 — Ebru Toker,1* Nursel Elcioglu,2 Eda Ozcan,1 Ozlem Yenice,1 and Mehdi Ogut1. 1Department of Ophthalmology, Marmara University, Medical School, Turkey.
Nursel Elcioglu - Academia.edu
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Academia.edu is a place to share and follow research.
Elcioglu, Nursel | DeepDyve
www.deepdyve.com
2, Luc De Catte 3, Nursel Elcioglu 4, Michael T. Gabbett 5,6, Louanne Hudgins 7, Jane A. Hurst 8, Fernanda Sarquis Jehee 9, Christine Oley ...
Antenatal diagnosis of velocardiofacial syndrome by 3D ultrasonography
www.degruyter.com
Alin Basgul 1 / Zehra Nese Kavak 2 / Esin Kotiloglu 3 / Ipek Akman 4 / Figen Akalin 5 / Nursel Elcioglu 6 / Aydın Sav
Wissenschaftliche Veröffentlichungen
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations...
www.sciencedirect.com
Ben Neriah, Fiona Stewart, Nursel Elcioglu, Tareq Hindi, Martine Le Merrer, ...
Novel MASP1 mutations are associated with an expanded ...Orphanet Journal of Rare Diseases
ojrd.biomedcentral.com
von T Atik · · Zitiert von: 48 — Nursel Elcioglu & Gulsen A. Tayfun. Department of Ophthalmology, Ataturk Teaching and Research Hospital, Katip Celebi University, Izmir, ...
Carpenter syndrome: extended RAB23 mutation spectrum ...Archive ouverte HAL
hal.science
von AO Wilkie · · Zitiert von: 40 — Andrew Om Wilkie 1, * Dagan Jenkins 2 Gareth Baynam 3 Luc de Catte 4Nursel Elcioglu 5 Michael Gabbett 6 Louanne Hudgins 7 Jane A Hurst 8 Fernanda Sarquis ...
Developmental genomics of limb malformations: Allelic ...ScienceDirect
www.sciencedirect.com
von R Duan · · Zitiert von: 2 — Nursel Elcioglu , Débora R. Bertola , Alper Gezdirici 13 , Haowei Du 1 , Jawid M. Fatih 1 , Christopher M. Grochowski 1
Veröffentlichungen allgemein
Genetic and Mutational Analyses of a Large Multiethnic Bardet Core
core.ac.uk
Nursel Elcioglu,7 Jamal Raza,8 Michael O. Woods,9 Jane S. Green,9 Patrick S. Parfrey,9. William S. Davidson,10 and James R. Lupski1,4. Departments of ...
Molecular Analysis of Turkish Maroteaux-Lamy Patients and...
link.springer.com
Nursel Elcioglu • Mehmet Nuri Özbek • Deniz K¨or •. Elisabetta Lenzini • Maurizio Scarpa • Rosella Tomanin. Received: 25 May Revised: ...
Dysosteosclerosis is also caused by TNFRSF11A mutation.MediFind
www.medifind.com
— Long Guo, Nursel Elcioglu, Ozge Karalar, Mert Topkar, Zheng Wang, Yuma Sakamoto, Naomichi Matsumoto, Noriko Miyake, Gen Nishimura, ...
Genetic and Mutational Analyses of a Large Multiethnic ...CORE
core.ac.uk
von PL Beales · · Zitiert von: 103 — Nursel Elcioglu,7 Jamal Raza,8 Michael O. Woods,9 Jane S. Green,9 Patrick S. Parfrey,9. William S. Davidson,10 and James R. Lupski1,4.
Artikel & Meinungen
IFT80, which encodes a conserved intraflagellar transport protein, is...
www.nature.com
Brief Communication
Sonstiges
Yavuz Bayram, Janson J. White, Nursel Elcioglu, Megan TSlidePlayer
slideplayer.com
Presentation on theme: "Yavuz Bayram, Janson J. White, Nursel Elcioglu, Megan T"— Presentation transcript: · 1 REST Final-Exon-Truncating Mutations Cause ...
Çapa Uzman Hekim - Yahoo Groups
groups.yahoo.com
_____ From: [] On Behalf Of Nursel Elcioglu (by way of Nursel ...
Nursel Elcioglu's research works | Marmara University ...ResearchGate
www.researchgate.net
Nursel Elcioglu's 5 research works with 27 citations and 686 reads, including: Back Cover, Volume 40, Issue 8.
Eye: Elcioglu, Nursel - Expertscape.com
www.expertscape.com
Medical and scientific articles about Eye, written by Nursel Elcioglu
"Mutations in FKBP10 cause recessive osteogenesis ...DIAL@UCLouvain
dial.uclouvain.be
von BP Kelley · · Zitiert von: 176 — Andy Willaert,3 Nursel Elcioglu,5 Lionel Van Maldergem,6 Christine Verellen-Dumoulin,7 Yves Gillerot,7. Dobrawa Napierala,1 Deborah Krakow,8 ...
Altmetric – A role for repressive complexes and H3K9 di-methylation...
oxfordjournals.altmetric.com
Louise F. Porter, Giorgio G. Galli, Sally Williamson, Julian Selley, David Knight, Nursel Elcioglu, Ali Aydin, Mustafa Elcioglu, Hanka Venselaar, Anders H. Lund, ...
A family with Symphalangism syndrome. - DocumentGale
go.gale.com
Tabakci, Burcu, and Huriye Nursel Elcioglu. "A family with Symphalangism syndrome." Erciyes Medical Journal, vol. 41, no. S1, June 2019, p Gale Academic ...
A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical...
pubmed.ncbi.nlm.nih.gov
... Tarik Kirkgoz , Sare Betul Kaygusuz , Yasemin Gokdemir , Huriye Nursel Elcioglu , Tulay Guran , Abdullah Bereket , Pinar Ata , Serap Turan ...
A role for repressive complexes and H3K9 di-methylation in...
www.research.manchester.ac.uk
author = "Porter, {Louise F} and Galli, {Giorgio G} and Sally Williamson and Julian Selley and David Knight and Nursel Elcioglu and Ali Aydin and Mustafa ...
A family with Symphalangism syndrome.go.gale.com › i.do
go.gale.com
Authors: Burcu Tabakci and Huriye Nursel Elcioglu. Date: June From: Erciyes Medical Journal(Vol. 41, Issue S1). Publisher: KARE Publishing. Document ...
AJMG - PartA / DOI: ajmg.a Centrum ...www.cmgg.be › over-ons › nieuws
www.cmgg.be
Sheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, Sujatha Jagadeesh, Dhanya Yesodharan, Beena Suresh, Serap Turan, Sofie Symoens, Fransiska ...
Antenatal diagnosis of velocardiofacial syndrome by 3D ...Grow Kudos
www.growkudos.com
... Ipek Akman, Figen Akalin, Figen Akalin, Nursel Elcioglu, Nursel Elcioglu, Aydın Sav, Aydın Sav. Journal of Perinatal Medicine, January 2006, De Gruyter.
JCI - Citations to RAP1-mediated MEK/ERK pathway defects in Kabuki...
www.jci.org
... Siddharth Banka, Andrea Kranz, Martin Zenker, Dagmar Wieczorek, Nursel Elcioglu, Paolo Prontera, Stanislas Lyonnet, Thomas Meitinger, A. Francis Stewart, ...
Carpenter syndrome: Extended RAB23 mutation spectrum ...Murdoch University
researchportal.murdoch.edu.au
von D Jenkins · · Zitiert von: 40 — Dagan Jenkins 1, Gareth Baynam 2, Luc De Catte 3, Nursel Elcioglu 4, Michael T. Gabbett 5,6, Louanne. Hudgins 7, Jane A. Hurst 8, ...
Decreased subfoveal choroidal thickness and failure of...
pubmed.ncbi.nlm.nih.gov
This study for the first time demonstrated that CT is decreased in patients with OCA at the subfoveal region. These data combined with the underdevelopment of...
Successful treatment of pityriasis lichenoides chronica with...
escholarship.org
Nursel Elcioglu. 2. , Gabriele Richard. 3. ,. Cuyan Demirkesen. 4. Dermatology Online Journal 22 (5): Marmara University, School of ...
Defective Escape Behavior in DEAH-Box RNA Helicase Mutants ...Journal of Neuroscience
www.jneurosci.org
... Asuman Koparir, Mehmet Bugrahan Duz, Emre Kirat, Elif Fenercioglu, Hakan Ulucan, Mehmet Seven, Tulay Guran, Nursel Elcioglu, Mahmut Selman Yildirim, ...
Carpenter syndrome: extended RAB23 mutation spectrum and analysis of...
hal.archives-ouvertes.fr
Carpenter syndrome, a rare autosomal recessive disorder characterized by a combination of craniosynostosis, polysyndactyly, obesity, and other congenital...
Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck...
lib.ugent.be
... Willaert AU - Nursel Elcioglu AU - Lionel Van Maldergem AU - Christine Verellen-Dumoulin AU - Yves Gillerot AU - Dobrawa Napierala AU - Deborah Krakow ...
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and...
www.research.manchester.ac.uk
author = "Yun Li and Barbara Pawlik and Nursel Elcioglu and Mona Aglan and H{\"u}lya Kayserili and G{\"o}khan Yigit and Ferda Percin and Frances Goodman ...
Verwandte Suchanfragen zu Nursel Elcioglu
| Mehmet Nuri Paul Perry Mona Aglan | Barbara Pawlik Dagmar Wieczorek Gabriele Richard | Kerstin Becker Mert Karakaya Harald Ehrhardt |
Personen Vorname "Nursel" (261) Name "Elcioglu" (3) |
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