Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array-based comparative genomic hybridization

✍ Scribed by Shin Hayashi; Masae Ono; Yoshio Makita; Issei Imoto; Shuki Mizutani; Johji Inazawa

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 203 KB
• Volume: 143A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.31737