Subject
Genetics(clinical),Genetics,General Medicine
Reference8 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. Silver-like syndrome and a small deletion on chromosome 13;Wahlström;Acta Paediatr.,1993
3. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3;Amor;Am. J. Med. Genet.,2005
4. Facial asymmetry, cardiovascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome: a microdeletion/duplication in 13q;Maas;Genet. Couns.,2006
5. Identification of two novel chromosome regions associated with isolated growth hormone deficiency;Cody;J. Pediatr. Endocrinol. Metab.,2010