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Results 1 - 10 of 16 for Lissencephaly 4
  1. ... j.ejpn.2009.01.005. Epub 2009 Mar 4. Citation on PubMed
  2. ... Dec 16. Citation on PubMed Wynshaw-Boris A. Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development. Clin Genet. 2007 Oct;72(4):296-304. doi: 10.1111/j.1399-0004. ...
  3. ... kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Am J Hum Genet. 2003 Apr;72(4):918-30. doi: 10.1086/374320. Epub 2003 ...
  4. ... kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Am J Hum Genet. 2003 Apr;72(4):918-30. doi: 10.1086/374320. Epub 2003 ...
  5. ... on PubMed Kato M, Dobyns WB. X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". J Child Neurol. 2005 Apr;20(4):392-7. doi: 10.1177/08830738050200042001. Citation on ...
  6. ... on PubMed Kato M, Dobyns WB. X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". J Child Neurol. 2005 Apr;20(4):392-7. doi: 10.1177/08830738050200042001. Citation on ...
  7. ... Hourihane JO, Martin ND, Walsh CA. Autosomal recessive lissencephaly with ... Biochem Cell Biol. 2012 Sep;44(9):1501-4. doi: 10.1016/j.biocel.2012.06.002. ...
  8. ... neuronal migration causes a brain abnormality called cobblestone lissencephaly, in which the surface of the ... 4-phosphate cytidylyltransferase-like protein 4-diphosphocytidyl-2C-methyl- ...
  9. ... condition typically have a brain abnormality called cobblestone lissencephaly, in which the surface of the brain lacks ... that this problem with neuronal migration causes cobblestone lissencephaly in children with Walker-Warburg syndrome. Less is ...
  10. ... usually causes a more severe condition called isolated lissencephaly sequence (ILS). Most males with subcortical band heterotopia ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov LISSENCEPHALY, X-LINKED, 1; LISX1 LISSENCEPHALY 1; LIS1 PubMed ...
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