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Items: 16

1.

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.

Reiner O, Carrozzo R, Shen Y, Wehnert M, Faustinella F, Dobyns WB, Caskey CT, Ledbetter DH.

Nature. 1993 Aug 19;364(6439):717-21.

PMID:
8355785
2.

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
3.

Murine modelling of classical lissencephaly.

Gambello MJ, Hirotsune S, Wynshaw-Boris A.

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

PMID:
10369882
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.

6.
7.

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
8.

The role of cytoplasmic dynein in the human brain developmental disease lissencephaly.

Vallee RB, Faulkner NE, Tai CY.

Biochim Biophys Acta. 2000 Mar 17;1496(1):89-98. Review.

9.

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
10.

Norman-Roberts syndrome: clinical and molecular studies.

Iannetti P, Schwartz CE, Dietz-Band J, Light E, Timmerman J, Chessa L.

Am J Med Genet. 1993 Aug 1;47(1):95-9. Review.

PMID:
8368261
11.

Lissencephaly and other malformations of cortical development: 1995 update.

Dobyns WB, Truwit CL.

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

PMID:
7477752
12.

[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
13.

Abnormal cortical development; towards elucidation of the LIS1 gene product function (review).

Reiner O, Sapir T.

Int J Mol Med. 1998 May;1(5):849-53. Review.

PMID:
9852306
14.

Cell migration and cerebral cortical development.

Golden JA.

Neuropathol Appl Neurobiol. 2001 Feb;27(1):22-8. Review.

PMID:
11298998
15.

[Subcortical laminal heterotopia and lissencephaly: cerebral malformations of X-linked inheritance].

Pinard JM, Desguerre I, Motte J, Dulac O, Ponsot G.

Rev Neurol (Paris). 1995 Mar;151(3):171-6. Review. French.

PMID:
7676153
16.

LIS1-Associated Lissencephaly/Subcortical Band Heterotopia.

Dobyns WB, Das S.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2009 Mar 3 [updated 2014 Aug 14].

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