A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes

✍ Scribed by Adam Shlien; Berivan Baskin; Maria Isabel W. Achatz; Dimitrios J. Stavropoulos; Kim E. Nichols; Louanne Hudgins; Chantal F. Morel; Margaret P. Adam; Nataliya Zhukova; Lianne Rotin; Ana Novokmet; Harriet Druker; Mary Shago; Peter N. Ray; Pierre Hainaut; David Malkin

• Book ID: 113422936
• Publisher: American Society of Human Genetics
• Year: 2010
• Tongue: English
• Weight: 860 KB
• Volume: 87
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1016/j.ajhg.2010.10.007