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22q11 deletion and polymicrogyria--cause or coincidence?
S Worthington1, A Turner, J Elber
1Department of Medical Genetics, Sydney Children's Hospital, Australia.
Clinical Dysmorphology
|August 24, 2000
Abstract:
We report a familial case of velocardiofacial syndrome (VCFS) with polymicrogyria to provide further support for the association of disorders of cortical development with del(22q11) syndromes.
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