Chromosomal Abnormalities and Epilepsy: A Review for Clinicians and Gene Hunters
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1528-1157.2002.19498.x/fullpdf
Reference228 articles.
1. Precise localization of NF1 to 17q11.2 by balanced translocation.;Ledbetter;Am J Hum Genet,1989
2. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.;Koenig;Cell,1987
3. Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2.;Riazi;Genomics,1999
4. Human cytogenetics database.
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