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Items: 14

1.

Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.

Ledbetter SA, Kuwano A, Dobyns WB, Ledbetter DH.

Am J Hum Genet. 1992 Jan;50(1):182-9.

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.

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, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2009 Mar 3 [updated 2014 Aug 14].

4.

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
5.

Murine modelling of classical lissencephaly.

Gambello MJ, Hirotsune S, Wynshaw-Boris A.

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

PMID:
10369882
6.

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
7.

The neurogenetics of lissencephaly.

Dobyns WB.

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

PMID:
2646523
8.

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
9.

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
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.
13.

[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
14.

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.

Guerrini R, Carrozzo R.

Seizure. 2002 Apr;11 Suppl A:532-43; quiz 544-7. Review.

PMID:
12185771

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