Author:
Mantel Anne,Leonard Claude,Husson Béatrice,Miladi Najoua,Tardieu Marc,Landrieu Pierre
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference10 articles.
1. De Rijk-van Andel JF, Arts WFM, Barth PG, Loonen MCB (1990) Diagnostic features and clinical signs of 21 patients with type 1 Lissencephaly. Dev Med Child Neurol 32:707–717
2. De Rijk-van Andel JF, Catsman-Berrevoets CE, Halley DJJ, Wesby-van Swaay, Niermeijer ME, Oostra BA (1991) Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13. Hum Genet 87:509–510
3. Dobyns WB (1989) The neurogenetics of Lissencephaly. Neurol Clin 7:89–105
4. Dobyns WB, Gilbert EF, Opitz JM (1985) Further comments on the Lissencephaly syndrome. Am J Med Genet 18:509–526
5. Dobyns WB, Curry CJR, Hoyme HE, Turlington L, Ledbetter DH (1991) Clinical and molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet 48:584–594
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献