Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 14

1.

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH.

JAMA. 1993 Dec 15;270(23):2838-42. Review.

PMID:
7907669
2.

Murine modelling of classical lissencephaly.

Gambello MJ, Hirotsune S, Wynshaw-Boris A.

Neurogenetics. 1999 Apr;2(2):77-86. Review.

PMID:
10369882
3.

LIS1-Associated Lissencephaly/Subcortical Band Heterotopia.

Dobyns WB, Das S.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2009 Mar 3 [updated 2014 Aug 14].

4.

Genetic factors in lissencephaly syndromes: a review.

Miny P, Holzgreve W, Horst J.

Childs Nerv Syst. 1993 Nov;9(7):413-7. Review.

PMID:
8306358
5.

Lissencephaly and the molecular basis of neuronal migration.

Kato M, Dobyns WB.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R89-96. Review.

PMID:
12668601
6.

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.

Chen CP, Chang TY, Guo WY, Wu PC, Wang LK, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W.

Gene. 2013 Dec 10;532(1):152-9. doi: 10.1016/j.gene.2013.09.044. Epub 2013 Sep 19. Review.

PMID:
24055730
7.

Lissencephaly and other malformations of cortical development: 1995 update.

Dobyns WB, Truwit CL.

Neuropediatrics. 1995 Jun;26(3):132-47. Review.

PMID:
7477752
8.

X-linked malformations of neuronal migration.

Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, Walsh CA, Truwit CL.

Neurology. 1996 Aug;47(2):331-9. Review.

PMID:
8757001
9.

[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. Review. French.

PMID:
17571022
10.
11.

Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).

Cardoso C, Leventer RJ, Dowling JJ, Ward HL, Chung J, Petras KS, Roseberry JA, Weiss AM, Das S, Martin CL, Pilz DT, Dobyns WB, Ledbetter DH.

Hum Mutat. 2002 Jan;19(1):4-15. Review.

PMID:
11754098
12.

Diagnostic features and clinical signs of 21 patients with lissencephaly type 1.

de Rijk-van Andel JF, Arts WF, Barth PG, Loonen MC.

Dev Med Child Neurol. 1990 Aug;32(8):707-17. Review.

PMID:
2210085
13.

[Chromosome arm 17p13.3: could HIC1 be the one ?].

Chopin V, Leprince D.

Med Sci (Paris). 2006 Jan;22(1):54-61. Review. French.

14.

The neurogenetics of lissencephaly.

Dobyns WB.

Neurol Clin. 1989 Feb;7(1):89-105. Review.

PMID:
2646523

Supplemental Content

Support Center