Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration

• Main Authors: González Eva (Author), Vilardell Mireia (Author), del Campo Miguel (Author), Cuscó Ivon (Author), Gener Blanca (Author), Galán Enrique (Author), Toledo Laura (Author), Pérez-Jurado Luis A (Author)
• Format: Book
• Published: BMC, 2008-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterized by specific facial features, mild to moderate mental retardation, postnatal growth delay, skeletal abnormalities, and unusual dermatoglyphic patterns with p...