Clinical characterization of a girl with trisomy 20q13.2qter and monosomy 13q33.1qter: Delineating phenotype-genotype correlations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference18 articles.
1. Partial trisomy 20q in a newborn with dextrocardia;Addor;Genet Couns,2002
2. 13q Deletion and central nervous system anomalies: Further insights from karyotype-phenotype analyses of 14 patients;Ballarati;J Med Genet,2007
3. Detection of low-level mosaicism by array CGH in routine diagnostic specimens;Ballif;Am J Med Genet Part A,2006
4. Preliminary definition of a “critical region” of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature;Brown;Am J Med Genet,1993
5. The 13q-syndrome: The molecular definition of a critical deletion region in band 13q32;Brown;Am J Hum Genet,1995
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