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

• Main Authors: Lin Lung-Huang (Author), Hung Kun-Long (Author), Cheong Mei-Leng (Author), Huang Cheng-Hung (Author), Yang Chen (Author), Yu Yeong-Seng (Author), Chien Chih-Cheng (Author), Huang Huei-Chen (Author), Chen Chan-Wei (Author), Huang Chi-Jung (Author)
• Format: Book
• Published: BMC, 2009-02-01T00:00:00Z.
• Subjects: article
• Online Access: 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...