Clinical and molecular genetic findings in five patients with Miller-Dieker syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb03951.x/fullpdf
Reference9 articles.
1. Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction;Batanian;Hum Genet,1990
2. Dinucleotide repeat polymorphism mapping to the critical region for lissencephaly (17p13.3);Carrozzo;Hum Molec Genet,1993
3. Clinical and molecular diagnosis of Miller-Dieker syndrome;Dobyns;Am J Hum Genet,1991
4. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13;Dobyns;JAMA,1993
5. Detection of deletions and cryptic translocations in Miller-Dicker syndrome by in situ hybridization;Kuwano;Am J Hum Genet,1991
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