1
0
0
(1 - 25 from 32
)
The aorta is torn apart in the Marfan syndrome | (e) Science News
esciencenews.com
In the current edition of the Deutsches Ärzteblatt International (Dtsch Arztebl Int 2008; 105[27]: ), the human geneticist Mine Arslan-Kirchner from Hannover
DocInsider: Profil von Dr. med. Mine Arslan-Kirchner
Dr. med. Arslan-Kirchner in Hannover, Fachärztin für Kinder- und Jugendmedizin - Arztsuche
Priv.-Doz. Dr. Mine Arslan-Kirchner (Ärztin, Humangenetikerin,...
www.jameda.de
Priv.-Doz. Dr. Mine Arslan-Kirchner in Hannover ➤ Ärztin, Humangenetikerin, Kinderärztin ✓ Erfahrungsberichte echter Patienten ✓ Telefonnummer,...
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye...
www.cell.com
Shauna Heeger. George Sabatakos. Suneel Apte. William N. Adkins. Jeremy Allgrove. Mine Arslan-Kirchner. Jennifer A. Batch. Peter Beighton.
Researchgate: Mine Arslan-Kirchner
Hannover, Niedersachsen, Germany
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and...
biblio.ugent.be
Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes. Mine Arslan-Kirchner, Joerg T Epplen, Laurence ...
Klinik und Genetik des Marfan-Syndroms - Mine Arslan-Kirchner -...
books.google.de
Front Cover. Mine Arslan-Kirchner · 0 Reviewshttp://books.google.com/books/about/Klinik_und_Genetik_des_Marfan_Syndroms.html?id=xgG8tgAACAAJ
Induzierung der Hyperphenylalaninämie und Phenylketonurie bei der...
books.google.de
Mine Arslan-Kirchner pages. 0 Reviewshttp://books.google.com/books/about/Induzierung_der_Hyperphenylalanin%C3%A4mie_u.html?id= ...
Clinical and molecular study of 320 children with Marfan syndrome and...
biblio.ugent.be
... Christine Binquet, Elodie Gautier, Bertrand Chevallier, Frederic Huet, Bart Loeys UGent, Eloisa Arbustini, Karin Mayer, Mine Arslan-Kirchner, ...
Cardiovascular manifestations in men and women carrying a FBN1 ...academic.oup.com › eurheartj › article-abstract
academic.oup.com
Aug 13, · ... Anne H. Child, Bart L. Loeys, Christine Binquet, Elodie Gautier, Eloisa Arbustini, Karin Mayer, Mine Arslan-Kirchner, Chantal Stheneur, ...
Clinical utility gene card for: Marfan syndrome type 1 and PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Mine Arslan-Kirchner , Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, Guillaume Jondeau, Bart Loeys, ...
TGFBR3 variation is not a common cause of Marfan-like syndrome and...
www.ncbi.nlm.nih.gov
Krishna K Singh, 1, 2 Joerg Schmidtke, 1 Britta Keyser, 1 and Mine Arslan-Kirchner 1
TGFBR3 variation is not a common cause of Marfan-like syndrome ...jnrbm.biomedcentral.com › articles
jnrbm.biomedcentral.com
Feb 2, · Krishna K Singh, Joerg Schmidtke, Britta Keyser & Mine Arslan-Kirchner. Division of Cardiac Surgery, St. Michael's Hospital, Toronto, Canada.
The Importance of Genetic Testing in the Clinical Management of...
www.ncbi.nlm.nih.gov
The Importance of Genetic Testing in the Clinical Management of Patients with Marfan Syndrome and Related Disorders. Mine Arslan-Kirchner ...
Google Groups: European Journal of Human Genetics - Table of Contents alert ...
: ... Loeys-Dietz syndrome (_TGFBR1/2_) and related phenotypes Mine Arslan-Kirchner, Jörg T Epplen, Laurence Faivre, Guillaume Jondeau, Jörg Schmidtke, ...
Wikipedia: Marfan-Syndrom – Wikipedia
Mine Arslan-Kirchner, Yskert von Kodolitsch, Jörg Schmidtke: Genetische Diagnostik beim Marfan-Syndrom und verwandten Erkrankungen: ...
Clinical utility gene card for: Hereditary thoracic aortic Naturewww.nature.com › ... › clinical utility gene card
www.nature.com
Oct 28, · Mine Arslan-Kirchner, Anna Dierking, Britta Keyser & Jörg Schmidtke. IRCCS Fondazione Policlinico San Matteo, Pavia, Italy. Eloisa Arbustini.
nature.com search
www.nature.com
Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, Guillaume Jondeau
Dr. med. Mine Arslan-Kirchner Humangenetik, Kinder-und Jugendmedizin...
www.sporlife.net
Dr. med. Mine Arslan-Kirchner - Hannover / Almanya Muayenehane Adres ve Telefon Bilgilerinin Yer Aldığı Sağlık Sitesi
Clinical and molecular study of 320 children with marfan syndrome ...moh-it.pure.elsevier.com › publications › clinical-and-molecular-study-of-...
moh-it.pure.elsevier.com
... Karin Mayer, Mine Arslan-Kirchner, Anatoli Kiotsekoglou, Paolo Comeglio, Maurizia Grasso, Dorothy J. Halliday, Christophe Beroud, Claire Bonithon-Kopp
Clinical utility gene card for: Hereditary Archive ouverte HALhal.archives-ouvertes.fr › hal
hal.archives-ouvertes.fr
Dec 21, · Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Philippe Charron, Anne Child, et al.. Clinical utility gene card for: Hereditary ...
Nascer e Crescer - Revista do Hospital de Crianças Maria Pia -...
www.scielo.oces.mctes.pt
Feliubadaló L., Bisceglia L., Font M., Dello Strologo L., Beccia E., mine Arslan-kirchner., et al. Recombinant Families Locate the Gene for Non-Type I Cystinuria ...
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye...
www.infona.pl
Mine Arslan-Kirchner. autor. Jennifer A. Batch. autor. Peter Beighton. autor. Graeme C.M. Black. autor. Richard G. Boles. autor. Laurence M. Boon. autor.
Clinical utility gene card for: Marfan syndrome type 1 and related...
www.bionity.com
Authors: Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Jörg Epplen, ...
Clinical utility gene card for: Hereditary thoracic aortic aneurysm...
moh-it.pure.elsevier.com
Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Philippe Charron, Anne H. Child, Gwenaelle Collod-Beroud, Julie De Backer, Anne ...
All web results to the name "Mine Arslan"
Related search requests for Mine Arslan
| Catherine Boileau Philippe Charron Cemal Gülpinarli | Sevgi Dunyasi |
Person "Arslan" (16) Forename "Mine" (1840) Name "Arslan" (3860) |
sorted by relevance / date