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Teilnehmende Kliniken
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Friedreich Ataxie. Klinik und Poliklinik für Neurologie der Universität Regensburg , Herr Dr. Uyanik -regensburg.dex.
Books & Literature
heiBIB: Behnecke, Anne
katalog.ub.uni-heidelberg.de
Ana Beleza-Meireles, Goekhan Uyanik, Sandra Janssens, Eugen Boltshauser, ...
47 patients with FLNA associated periventricular nodular heterotopia
biblio.ugent.be
Goekhan Uyanik, Sandra Janssens UGent, Eugen Boltshauser, ...
Goekhan Uyanik | XanEdu Customization Platform
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Author: Goekhan Uyanik. Results. Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation Springer ...
Related Documents
EBSCOhost | | Heterozygous mutations in SIX3 and SHH are...
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Ute Hehr • Daniel E. Pineda-Alvarez • Goekhan Uyanik • Ping Hu • Nan Zhou • Andreas Hehr •. Chayim Schell-Apacik • Carola Altus • Cornelia ...
Familial West syndrome and dystonia caused by an Aristaless related...
www.deepdyve.com
Gabriele Wohlrab Æ Goekhan Uyanik Æ Claudia Gross. Ute Hehr Æ Ju. ¨. rgen Winkler Æ Bernhard Schmitt. Eugen Boltshauser. Familial West syndrome and ...
Heterozygous mutations in SIX3 and SHH are associated with...
www.deepdyve.com
with schizencephaly and further expand the clinical spectrum. of holoprosencephaly. Ute Hehr. •. Daniel E. Pineda-Alvarez. •. Goekhan Uyanik. •. Ping Hu.
Scientific Publications
47 patients with FLNA associated periventricular nodular heterotopia...
ojrd.biomedcentral.com
... Franziska Mueller,; Ulrike Siebers-Renelt,; Ana Beleza-Meireles,; Goekhan Uyanik,; Sandra Janssens,; Eugen Boltshauser,; Juergen Winkler ...
Publications
Novel POMGnT1 mutations define broader phenotypic spectrum of...
link.springer.com
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease. Ute Hehr & Goekhan Uyanik & Claudia Gross &.
Goekhan Uyanik's Research | CureHunter
www.curehunter.com
Goekhan Uyanik Selected Research. Goekhan Uyanik Research Topics. Disease. 1, Paraplegia (Spastic Paraplegia) , Walker-Warburg Syndrome
Mitotic impairment by doublecortin is diminished by doublecortin...
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Volkswagen Foundation Research GroupUniversity of Regensburg. Goekhan Uyanik, ...
Reports & Statements
eBOOk--- GeneReviews : 네이버 블로그
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... September 8, 2005Last Update: August 18, 2009; D; DCX-Related Disorders Goekhan Uyanik, Ludwig Aigner, Sebastien Couillard-Despres, ...
Miscellaneous
Goekhan Uyanik
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Search results for: Goekhan Uyanik ... Sebastien Couillard-Despres, Goekhan Uyanik, Sonja Ploetz, Claudia Karl, more · Neurogenetics > > 5 > 2.
A genealogy of the Nye family, Volume 11907, Robert Glen Nye,...
garzonls.surge.sh
6 Ute Hehr , Daniel E. Pineda-Alvarez , Goekhan Uyanik , Ping Hu , Nan Zhou , Andreas Hehr , Chayim Schell-Apacik , Carola Altus , Cornelia Daumer-Haas ...
Mutations in SPG11 are frequent in autosomal recessive spastic...
academic.oup.com
Vardiela Meiner, Goekhan Uyanik, Anne Kjersti Erichsen, Imed ...
OPUS FAU | 47 patients with FLNA associated periventricular nodular...
opus4.kobv.de
... Katharina Diepold, Isolde Schreyer, Matthias K. Bernhard, Franziska Mueller, Ulrike Siebers-Renelt, Ana Beleza-Meireles, Goekhan Uyanik, ...
Mitotic impairment by doublecortin is diminished by doublecortin...
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Sebastien Couillard-Despres, Goekhan Uyanik, Sonja Ploetz, Claudia Karl, Hartmut Koch, Juergen Winkler, Ludwig Aigner. Neurogenetics 2004, 5 (2):
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