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News
Netzwerk-Profile
LinkedIn: Dr Mona Sabry Aglan - Deputy Head Of Division - National Research ...
Mona Aglan is a Professor of Clinical Genetics and Deputy Head of the Human Genetics and Genome Research Division at the National Research Centre ...
Bücher
Einen Moment, bitte...
www.hugendubel.de
Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian Family, Buch (kartoniert) von Alaaeldin Fayez, Mona Aglan, Mona El Ruby bei hugendubel.de. Portofrei bestellen oder in der Filiale abholen.
Osteogenesis Imperfecta: A Translational Approach to Brittle Bone...
books.google.de
OSX/SP7 Mutations and Osteogenesis Imperfecta JOSÉ ANTONIO CAPARRÓS-MARTÍN, MONA AGLAN, SAMIA TEMTAMY, VÍCTOR MARTÍNEZ-GLEZ, MARÍA ...
Bone Dysplasias: An Atlas of Genetic Disorders of Skeletal...
books.google.com.ua
The definitive guide to genetic bone disorders, now revised and expanded with glossy photographs and radiographs
Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian Family...
www.lap-publishing.com
Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian FamilyGenetics, We wrote this book for everyone...
Dokumente zum Namen
EBSCOhost | | A Novel Loss-of-Sclerostin Function Mutation...
web.a.ebscohost.com
Alaaeldin Fayez,1 Mona Aglan,2 Nora Esmaiel,1 Taher El Zanaty,3. Mohamed Abdel Kader,4 and Mona El Ruby2. 1 Molecular Genetics and ...
Clinical and molecular analysis in families with autosomal recessive...
www.deepdyve.com
Samia Temtamy,. 4. * and Mona Aglan. 4. *. 1. Instituto de Investigaciones Biome. ´. dicas, Consejo Superior de Investigaciones Cientı. ´. ficas-Universidad Auto.
Wissenschaftliche Veröffentlichungen
Publikationen | Humangenetik Uniklinik Köln
humangenetik.uk-koeln.de
Eine aktuelle Liste der Publikationen der Mitarbeiter des Instituts für Humangenetik der Uniklinik Köln. Informieren Sie sich jetzt!
Artikel & Meinungen
Biallelic mutations in SNX14 cause a syndromic form of cerebellar...
www.nature.com
Joseph Gleeson and colleagues report that biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy marked by lysosome-autophagosome...
Sonstiges
Mona Aglan | LinkedIn
www.linkedin.com
View Mona Aglan's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Mona Aglan discover inside ...
[kasrgroup82] Fw - Yahoo Groups
groups.yahoo.com
To: El-Kasr Group &>; Manal Micheal <nula_m @...>; Maha Zaki <dr_mahazaki@...>; Dr. Mona Aglan <drmona_aglan@.
Stream mo music | Listen to songs, albums, playlists for free on...
soundcloud.com
Play mo and discover followers on SoundCloud | Stream tracks, albums, playlists on desktop and mobile.
Stream Mona Aglan music | Listen to songs, albums, playlists for free...
soundcloud.com
Play Mona Aglan and discover followers on SoundCloud | Stream tracks, albums, playlists on desktop and mobile.
All Mona Aglan's Virtual Tours
www.propertypanorama.com
View all of Mona Aglan's
InstaView virtual tours.
Mona Aglan
www.infona.pl
Mona Aglan. Details · Publications ... Ranad Shaheen, Mona Aglan, Kim Keppler-Noreuil, Eissa Faqeih, more · The American Journal of ...
Publications | Human Genetics Uniklinik Köln
humangenetik.uk-koeln.de
Samia Temtamy, Mona Aglan, A. Kemal Topaloglu, Bernd Wollnik, Khalda Amr, Tarek H El-Badry, Gamal A Hosny, Nermine Salah Eldin, Mohammad Shboul, Mustafa Herdem, Junxian Ong, Bruno Reversade, Jingh Tian. Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations.
TRAINERINNENLISTE "ARGUMENTATIONSTRAINING GEGEN...
docplayer.org
Aglan Mona, Mag. a Innovia , Innsbruck / Appel Margit, Mag. a Katholische Sozialakademie Österreichs Schottenring 35/DG, Mehr
A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian...
www.proquest.com
Alaaeldin Fayez 1 and Mona Aglan 2 and Nora Esmaiel 1 and Taher El Zanaty 3 and Mohamed Abdel Kader 4 and Mona El Ruby 2. Academic Editor:Jozef ...
Altmetric – Biallelic mutations in SNX14 cause a syndromic form of...
www.altmetric.com
... R Koksal Ozgul, Mahmut Samil Sagıroglu, Matloob Azam, Samira Ismail, Mona Aglan, Laila Selim, Iman G Mahmoud, Sawsan Abdel-Hadi, Amera El Badawy, ...
Faculty of medicine - International Workshop on Consanguinity
www.medecine.unige.ch
Professor Mona Aglan. 15:00. Consanguinity in the South Asian Population: comparative study of Britain and Canada Mubasshir Ajaz. 15:20. Coffee break.
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and...
www.infona.pl
Mona Aglan. Departments of Clinical and Molecular Genetics, Division of Human Genetics & Genome Research, National... see all ...
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 ...
Middle East Journal of Medical Genetics : About us
www.mxe.eg.net
SamiaTemtamy. National Research Centre, Cairo, Egypt. Deputy Editor Amal Mahmoud National Research Centre, Cairo, Egypt. Associate Editors Mona Aglan
Mutations in WNT1 cause different forms of bone fragility - Citation...
fis-uke.de
... and Ekkehart Lausch and Tufan Cankaya and Caparrós-Martín, {José A} and Pablo Lapunzina and Samia Temtamy and Mona Aglan and Bernhard Zabel and ...
Region 9 Local Road Safety Peer Exchange - Safety | Federal Highway...
safety.fhwa.dot.gov
Alaska DOT & Public Facilities Business Phone: Business . Arizona. Mona Aglan-Swick
Robarts Vascular Research Publications | Robarts Research Institute |...
ir.lib.uwo.ca
... Mona Aglan, L. Damla Kotan, Gökhan Yigit, Husniye Canan, Barbara Pawlik, Gudrun Nürnberg, Emma L. Wakeling, Oliver W. Quarrell, Ingelore Baessmann, ...
Sendeschwerpunkt zum Tag der Sprachen am 26. September – FREIRAD...
www.freirad.at
FREIRAD Tirols einziges und erstes Freies Radio. Website mit dem aktuellen Programm, News, Infos zu Seminaren und einem Live Stream.
Specific variants in WDR35 cause a distinctive form of ellis-van...
moh-it.pure.elsevier.com
José A. Caparrós-martín ; Alessandro De Luca ; François Cartault ; Mona Aglan ; Samia Temtamy ; Ghada A. Otaify ; Mennat Mehrez ; María ...
Un nuevo gen en la lista de los causantes de los ‘huesos de cristal’
www.agenciasinc.es
La osteogénesis imperfecta también se produce por mutaciones en ‘BMP1’, que dificultan la formación de colágeno I funcionalmente maduro. Este nuevo...
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