Genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference23 articles.
1. Disease-causing mutations in the human genome;Antonarakis;Eur. J. Pediatr.,2000
2. Mutations in the CHD7 gene: the experience of a commercial laboratory;Bartels;Genet. Test. Mol. Biomarkers,2010
3. CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype;Bergman;J. Med. Genet.,2011
4. CHARGE association: an update and review for the primary pediatrician;Blake;Clin. Pediatr. (Phila.),1998
5. Trisomy 13 syndrome;Fukushima;Otol. Neurotol.,2008
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