Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome

• Principais autores: Lin Lung-Huang (Autor), Hung Kun-Long (Autor), Cheong Mei-Leng (Autor), Huang Cheng-Hung (Autor), Yang Chen (Autor), Yu Yeong-Seng (Autor), Chien Chih-Cheng (Autor), Huang Huei-Chen (Autor), Chen Chan-Wei (Autor), Huang Chi-Jung (Autor)
• Formato: Livro
• Publicado em: BMC, 2009-02-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Chromosome 22q11 deletion syndrome (22q11DS) causes a developmental disorder during the embryonic stage, usually because of hemizygous deletions. The clinical pictures of patients with 22q11DS vary because of polymorphisms: on averag...