L'épilepsie dans les aberrations chromosomiques
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference40 articles.
1. Chromosome imbalances associated with epilepsy;Schinzel;Am. J. Med. Genet.,2001
2. A G-band study of chromosomes in liveborn infants;Buckton;Ann. Hum. Genet.,1980
3. Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes;Riegel;Am. J. Med. Genet.,1999
4. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis;Blennow;Am. J. Med. Genet.,1996
5. Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome;Shapira;Am. J. Hum. Genet.,1997
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