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MID1 mutations in patients with X-linked Opitz G/BBB syndrome

โœ Scribed by Bianca Fontanella; Giorgio Russolillo; Germana Meroni


Book ID
102262078
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
237 KB
Volume
29
Category
Article
ISSN
1059-7794

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โœฆ Synopsis


Communicated by Arnold


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Communicated by Nancy B. Spinner Opitz G/BBB Syndrome (OS) is a multiple congenital anomaly disorder characterized by defects along the body midline. The disease is characterized by variable expressivity of signs that include hypertelorism, cleft lip and/or palate, laryngo-tracheo-esophageal abnorma