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3. Genotypically defined lissencephalies show distinct pathologies. Forman MS; Squier W; Dobyns WB; Golden JA J Neuropathol Exp Neurol; 2005 Oct; 64(10):847-57. PubMed ID: 16215456 [TBL] [Abstract][Full Text] [Related]
4. Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis. Leventer RJ; Pilz DT; Matsumoto N; Ledbetter DH; Dobyns WB Mol Med Today; 2000 Jul; 6(7):277-84. PubMed ID: 10859564 [TBL] [Abstract][Full Text] [Related]
5. Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia. Haverfield EV; Whited AJ; Petras KS; Dobyns WB; Das S Eur J Hum Genet; 2009 Jul; 17(7):911-8. PubMed ID: 19050731 [TBL] [Abstract][Full Text] [Related]
6. Potential mechanisms of mutations that affect neuronal migration in man and mouse. Walsh CA; Goffinet AM Curr Opin Genet Dev; 2000 Jun; 10(3):270-4. PubMed ID: 10826984 [TBL] [Abstract][Full Text] [Related]
7. Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered. Leventer RJ J Child Neurol; 2005 Apr; 20(4):307-12. PubMed ID: 15921231 [TBL] [Abstract][Full Text] [Related]
8. Missense mutations resulting in type 1 lissencephaly. Reiner O; Coquelle FM Cell Mol Life Sci; 2005 Feb; 62(4):425-34. PubMed ID: 15719169 [TBL] [Abstract][Full Text] [Related]
9. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing. Guerrini R; Carrozzo R Seizure; 2001 Oct; 10(7):532-43; quiz 544-7. PubMed ID: 11749114 [TBL] [Abstract][Full Text] [Related]
10. Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different. Viot G; Sonigo P; Simon I; Simon-Bouy B; Chadeyron F; Beldjord C; Tantau J; Martinovic J; Esculpavit C; Brunelle F; Munnich A; Vekemans M; Encha-Razavi F Am J Med Genet A; 2004 Apr; 126A(2):123-8. PubMed ID: 15057976 [TBL] [Abstract][Full Text] [Related]
11. Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. D'Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM; Palmini A; Costa da Costa J; Scheffer IE; Berkovic S; Guerrini R; Dravet C; Ono J; Gigli G; Federico A; Booth F; Bernardi B; Volpi L; Tassinari CA; Guggenheim MA; Ledbetter DH; Gleeson JG; Lopes-Cendes I; Vossler DG; Malaspina E; Franzoni E; Sartori RJ; Mitchell MH; Mercho S; Dubeau F; Andermann F; Dobyns WB; Andermann E Brain; 2002 Nov; 125(Pt 11):2507-22. PubMed ID: 12390976 [TBL] [Abstract][Full Text] [Related]
12. Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary. Mokánszki A; Körhegyi I; Szabó N; Bereg E; Gergev G; Balogh E; Bessenyei B; Sümegi A; Morris-Rosendahl DJ; Sztriha L; Oláh E J Child Neurol; 2012 Dec; 27(12):1534-40. PubMed ID: 22408144 [TBL] [Abstract][Full Text] [Related]
13. Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia. Delatycki MB; Leventer RJ Eur J Hum Genet; 2009 Jun; 17(6):701-2. PubMed ID: 19050725 [No Abstract] [Full Text] [Related]
14. Doublecortin functions at the extremities of growing neuronal processes. Friocourt G; Koulakoff A; Chafey P; Boucher D; Fauchereau F; Chelly J; Francis F Cereb Cortex; 2003 Jun; 13(6):620-6. PubMed ID: 12764037 [TBL] [Abstract][Full Text] [Related]
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16. [Genetic and clinical aspects of lissencephaly]. Verloes A; Elmaleh M; Gonzales M; Laquerrière A; Gressens P Rev Neurol (Paris); 2007 May; 163(5):533-47. PubMed ID: 17571022 [TBL] [Abstract][Full Text] [Related]
18. Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. Pilz DT; Kuc J; Matsumoto N; Bodurtha J; Bernadi B; Tassinari CA; Dobyns WB; Ledbetter DH Hum Mol Genet; 1999 Sep; 8(9):1757-60. PubMed ID: 10441340 [TBL] [Abstract][Full Text] [Related]
19. The unfolding story of two lissencephaly genes and brain development. Reiner O Mol Neurobiol; 1999; 20(2-3):143-56. PubMed ID: 10966119 [TBL] [Abstract][Full Text] [Related]
20. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Pilz DT; Matsumoto N; Minnerath S; Mills P; Gleeson JG; Allen KM; Walsh CA; Barkovich AJ; Dobyns WB; Ledbetter DH; Ross ME Hum Mol Genet; 1998 Dec; 7(13):2029-37. PubMed ID: 9817918 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]