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	21.	Novel human pathological mutations. Gene symbol: DCX. Disease: double cortex syndrome. [electronic resource] by Ellison, Jay Producer: 20110506 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	22.	[Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human]. [electronic resource] by Kielar, Michel Phan Dinh Tuy, Françoise Bizzotto, Sara Belvindrah, Richard Croquelois, Alexandre Francis, Fiona Producer: 20150424 In: Medecine sciences : M/S vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation. [electronic resource] by Kobayashi, Yu Magara, Shinichi Okazaki, Kenichi Komatsubara, Takao Saitsu, Hirotomo Matsumoto, Naomichi Kato, Mitsuhiro Tohyama, Jun Producer: 20170213 In: Brain & development vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia. [electronic resource] by Collins, Stephan C Uzquiano, Ana Selloum, Mohammed Wendling, Olivia Gaborit, Marion Osipenko, Maria Birling, Marie-Christine Yalcin, Binnaz Francis, Fiona Producer: 20200911 In: Journal of anatomy vol. 235 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Lissencephaly variant of band heterotopia: PET peeves. [electronic resource] by Shetty-Alva, Neetha Producer: 20080214 In: Pediatric neurology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia. [electronic resource] by Delatycki, Martin B Leventer, Richard J Producer: 20090901 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	[Prenatal diagnosis of fetal gray matter heteropia in one case and literature review]. [electronic resource] by Zhagn, Kui Li, Shengli Wen, Huaxuan Yuan, Ying Producer: 20160426 In: Nan fang yi ke da xue xue bao = Journal of Southern Medical University vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	28.	Ictal/interictal EEG patterns and functional neuroimaging findings in subcortical band heterotopia: report of three cases and review of the literature. [electronic resource] by Dericioglu, Nese Oguz, Kader Karli Ergun, Eser Lay Tezer, Fadime Irsel Saygi, Serap Producer: 20080410 In: Clinical EEG and neuroscience vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Somatic mutation, genomic variation, and neurological disease. [electronic resource] by Poduri, Annapurna Evrony, Gilad D Cai, Xuyu Walsh, Christopher A Producer: 20130716 In: Science (New York, N.Y.) vol. 341 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Recurrent KIF2A mutations are responsible for classic lissencephaly. [electronic resource] by Cavallin, Mara Bijlsma, Emilia K El Morjani, Adrienne Moutton, Sébastien Peeters, Els A J Maillard, Camille Pedespan, Jean Michel Guerrot, Anne-Marie Drouin-Garaud, Valérie Coubes, Christine Genevieve, David Bole-Feysot, Christine Fourrage, Cecile Steffann, Julie Bahi-Buisson, Nadia Producer: 20180221 In: Neurogenetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Sustained seizure freedom with transcutaneous vagal nerve stimulation in drug-resistant epilepsy caused by subcortical band heterotopias. [electronic resource] by von Wrede, Randi Moskau-Hartmann, Susanna Rüber, Theodor Helmstaedter, Christoph Surges, Rainer Producer: 20200218 In: Seizure vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Miller-Dieker Syndrome due to a 5.5-Mb 17p Deletion in a 17;Y Pseudodicentric Chromosome. [electronic resource] by Bellucco, Fernanda T Nunes, Natália Colovati, Mileny E S Malinverni, Andréa C M Caneloi, Thamy P Soares, Maria F A Perez, Ana B Melaragno, Maria I Producer: 20170929 In: Cytogenetic and genome research vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Long-term follow-up of type 1 lissencephaly: survival is related to neuroimaging abnormalities. [electronic resource] by de Wit, Marie-Claire Y de Rijk-van Andel, Jojanneke Halley, Dicky J Poddighe, Pino J Arts, Willem Frans M de Coo, Irenaeus F M Mancini, Grazia M S Producer: 20110610 In: Developmental medicine and child neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Double cortex syndrome in a male patient without lissencephaly. [electronic resource] by Rivero Rodríguez, D Scherle Matamoros, C Dicapua Sacoto, D Maldonado Samaniego, N Producer: 20210108 In: Neurologia vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Stumbling towards a diagnosis. [electronic resource] by Wakerley, B R Wilder-Smith, E P Yuki, N Producer: 20160201 In: Practical neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex. [electronic resource] by Bizzotto, Sara Uzquiano, Ana Dingli, Florent Ershov, Dmitry Houllier, Anne Arras, Guillaume Richards, Mark Loew, Damarys Minc, Nicolas Croquelois, Alexandre Houdusse, Anne Francis, Fiona Producer: 20190726 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Prenatal diagnosis of Miller-Dieker syndrome by ultrasound and molecular cytogenetic analysis. [electronic resource] by Lenzini, Elisabetta D'Ottavio, Giuseppina Città, Angelo Benussi, Daniela Gambel Petix, Vincenzo Pecile, Vanna Producer: 20080104 In: Clinical genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. [electronic resource] by Di Donato, Nataliya Timms, Andrew E Aldinger, Kimberly A Mirzaa, Ghayda M Bennett, James T Collins, Sarah Olds, Carissa Mei, Davide Chiari, Sara Carvill, Gemma Myers, Candace T Rivière, Jean-Baptiste Zaki, Maha S Gleeson, Joseph G Rump, Andreas Conti, Valerio Parrini, Elena Ross, M Elizabeth Ledbetter, David H Guerrini, Renzo Dobyns, William B Producer: 20190213 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Small Rho-GTPases and cortical malformations: fine-tuning the cytoskeleton stability. [electronic resource] by Cappello, Silvia Producer: 20130913 In: Small GTPases vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Rare Concurrence of Two Congenital Disorders: Miller-Dieker Syndrome and T-Cell Lymphopenia. [electronic resource] by Chee, Siew-Yin Guo, Jiun-Wen Huang, Chi-Jung Chien, Yin-Hsiu Lee, Yu-Chin Feng, Wen-Kan Producer: 20190701 In: Cytogenetic and genome research vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 158 results.