Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration
<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...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
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BMC,
2008-04-01T00:00:00Z.
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