Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Hamdan, Fadi F1"'
Autor:
Amrom, D., Tanyalcin, Ibrahim, Verhelst, H., Deconinck, N., Brouhard, Gary, Decarie, Jean-Claude, Tim, Vanderhasselt, Das, S., Hamdan, Fadi F1, Lissens, W., Michaud, Jacques, Jansen, Anna
Publikováno v:
CLINICAL GENETICS
Background: Dominant mutations in TUBB2B have been reported in patients with polymicrogyria. We further explore the phenotype associated with mutations in TUBB2B. Methods: Twenty patients with polymicrogyria (5 unilateral) were tested for mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ea215e6227b5b2ce0ed0d2e5029924d9
https://biblio.ugent.be/publication/5658787
https://biblio.ugent.be/publication/5658787
Autor:
Amrom, D., Tanyalcin, Ibrahim, Verhelst, Helene, Deconinck, N., Brouhard, Gary, Decarie, Jean-Claude, Tim, Vanderhasselt, Das, Soma, Hamdan, Fadi F1, Lissens, W., Michaud, Jacques, Jansen, Anna
Background: Dominant mutations in TUBB2B have been reported in patients with polymicrogyria. We further explore the phenotype associated with mutations in TUBB2B. Methods: Twenty patients with polymicrogyria (5 unilateral) were tested for mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::6e193b080a9cf71025c7c98dfa03bb2c
https://hdl.handle.net/20.500.14017/0658ca91-4000-4f12-b0ae-0602a297f150
https://hdl.handle.net/20.500.14017/0658ca91-4000-4f12-b0ae-0602a297f150