Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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2. Molecular analysis of 20 patients with 2q37.3 monosomy: Definition of minimum deletion intervals for key phenotypes;Aldred;J Med Genet,2004
3. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment;Anderlid;Eur J Hum Genet,2003
4. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p;Brown;Am J Hum Genet,1997
5. Clinical phenotype associated with terminal 2q37 deletion;Conrad;Clin Genet,1995
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