A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

✍ Scribed by B Auber; P Burfeind; S Herold; K Schoner; G Simson; R Rauskolb; H Rehder

• Book ID: 110888474
• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 241 KB
• Volume: 72
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/j.1399-0004.2007.00880.x