Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference41 articles.
1. Congenital eye malformations: clinical-epidemiological analysis of 1,124,654 consecutive births in Spain;Bermejo;Am J Med Genet,1998
2. Fragile site on chromosome 16 and the 16q syndrome;Brenholz;Am J Hum Genet,1982
3. Re-evaluation of GM 2346 from a del(16)(q22) to t(4;16)(q35;q22.1);Callen;Clin Genet,1990
4. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype;Callen;J. Med Genet,1993
5. De novo trisomy 16p;Carrasco Juan;Am J Med Genet,1997
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4. Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization;American Journal of Perinatology Reports;2011-03-18
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