Where I see patients (1)
Selected research
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A de novo int22h-1/int22h-2-flanked Xq28 deletion-associated preferential X-inactivation in a female with severe hemophilia B.
Pediatric blood & cancer
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Highly efficient capture approach for the identification of diverse inherited retinal disorders.
NPJ genomic medicine
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Genetic ancestry and diagnostic yield of exome sequencing in a diverse population.
NPJ genomic medicine
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- (415) 353-7800