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RE(ACT)2014Rare Diseases. 2nd International Congress on Research of Rare and Orphan Diseases. 5th to 8th March 2014, Gehry Building, Novartis Campus, Basel: Abstracts
Author(s) -
Benjamin D. Solomon,
F. Hadžiselimović,
N.O. Hadziselimovic,
P. Demougin,
Edward J. Oakeley,
Hartmut Engels,
Alexander M. Zink,
Eva Wohlleber,
Olaug K. Rødningen,
Kirstine Ravn,
Stefanie HeilmannHeimbach,
Julia Rehnitz,
N. Katzorke,
Cornelia Kraus,
Susanne Blichfeldt,
Peter M. Hoffmann,
Heiko Reutter,
F.F. Brockschmidt,
Martina KreißNachtsheim,
P. H. Vogt,
Trine Prescott,
Zeynep Tümer,
Jaimy Lee,
Zehra Oya Uyguner,
M. Kocaoğlu,
Güven Toksoy,
Seniha Başaran,
Hülya Kayserili,
C. Dubourg,
Frédérique BonnetBrilhault,
A. Toutain,
C. Mignot,
A. Jacquette,
A. Dieux,
M. Gérard,
M.-P. Beaumont-Epinette,
Sophie Julia,
Bertrand Isidor,
Matteo Rossi,
Sylvie Odent,
Claude Bendavid,
C Barthélémy,
Alain Verloès,
Valentin David,
O. M'hamdi,
Inès Ouertani,
Habiba Chaabouni-Bouhamed,
Satz Mengensatzproduktion,
Druckerei Stückle
Publication year - 2014
Publication title -
molecular syndromology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 36
eISSN - 1661-8777
pISSN - 1661-8769
DOI - 10.1159/000358504
Subject(s) - orphan drug , medicine , bioinformatics , biology

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