Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Malformations of Cortical Development and TUBB2B[original query] |
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| Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations. European journal of human genetics : EJHG 2012 Sep 20 (9): 995-8. Guerrini Renzo, Mei Davide, Cordelli Duccio Maria, Pucatti Daniela, Franzoni Emilio, Parrini Ele |
| Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development. Pediatric neurology 2019 9 103 27-34. Lee Sangbo, Kim Se Hee, Kim Borahm, Lee Seung-Tae, Choi Jong Rak, Kim Heung Dong, Lee Joon Soo, Kang Hoon-Ch |
| Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development Turkish journal of medical sciences 2020 Jul . Aksel KiliÇarslan Özge, Ataman Esra, GÜrsoy Semra, GÜrbÜz GÜrkan, Ünalp Aycan, GenÇpinar Pinar, OlgaÇ DÜndar NIhal, EdIzer SelvInaz, Ülgenalp Ayfer, GIray Bozkaya Özl |
| Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations. Seizure 2020 6 80 145-152. Accogli Andrea, Severino Mariasavina, Riva Antonella, Madia Francesca, Balagura Ganna, Iacomino Michele, Carlini Barbara, Baldassari Simona, Giacomini Thea, Croci Carolina, Pisciotta Livia, Messana Tullio, Boni Antonella, Russo Angelo, Bilo Leonilda, Tonziello Rosa, Coppola Antonietta, Filla Alessandro, Mecarelli Oriano, Casalone Rosario, Pisani Francesco, Falsaperla Raffaele, Marino Silvia, Parisi Pasquale, Ferretti Alessandro, Elia Maurizio, Luchetti Anna, Milani Donatella, Vanadia Francesca, Silvestri Laura, Rebessi Erika, Parente Eliana, Vatti Giampaolo, Mancardi Maria Margherita, Nobili Lino, Capra Valeria, Salpietro Vincenzo, Striano Pasquale, Zara Federi |
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