MID1 mutation screening in a large cohor
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Rosa Ferrentino; Maria Teresa Bassi; David Chitayat; Elisabetta Tabolacci; Germa
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Article
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2007
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John Wiley and Sons
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English
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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