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Lyons, Michael

One or more keywords matched the following items that are connected to Lyons, Michael

Item Type	Name
Academic Article	FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.
Academic Article	Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.
Concept	Abnormalities, Multiple
Academic Article	A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.

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