Subject
Genetics(clinical),Genetics,General Medicine
Reference7 articles.
1. 21 Mb deletion in chromosome band 13q22.2-q32.1 associated with mild/moderate psychomotor retardation, growth hormone insufficiency, short neck, micrognathia, hypotonia, dysplastic ears and other dysmorphic features;Grigori;Eur. J. Med. Genet.,2011
2. Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter;Kirchhoff;Am. J. Med. Genet.,2009
3. 13q deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients;Ballarati;J. Med. Genet.,2007
4. Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress;Quélin;Eur. J. Med. Genet.,2009
5. Silver-like syndrome and a small deletion on chromosome 13;Wahlström;Acta Paediatr.,1993
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