Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33935/fullpdf
Reference5 articles.
1. Features of trisomy 18 and 18p-syndromes in an infant with 45,XY,i(18q);Bass;Clin Genet,1979
2. DNA studies of mono- and pseudodicentric isochromosomes 18q;Bugge;Am J Med Genet Part A,2004
3. A new trisomic syndrome;Edwards;Lancet,1960
4. Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology;Froster-Iskenius;Clin Genet,1984
5. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18;Vianna-Morgante;J Med Genet,1976
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