A child with terminal 14q deletion syndrome: Consideration of genotype-phenotype correlations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32752/fullpdf
Reference19 articles.
1. Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals;DeScipio;Am J Med Genet Part A,2008
2. The r(14) syndrome. 3 new observations. [Le syndrome r(14). Trois nouvelles observations];Gilgenkrantz;Ann Genet,1984
3. Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2;Giorda;Hum Mutat,2007
4. Partial deletion of 14q and partial duplication of 14q in sibs: Testicular mosaicism for t(14q;14q) as a common mechanism;Masada;Am J Med Genet,1989
5. Terminal 14q32.33 deletion: Genotype-phenotype correlation;Maurin;Am J Med Genet Part A,2006
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