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Berry-Kravis, Elizabeth
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Berry-Kravis, Elizabeth
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Academic Article
Variable human phenotype associated with novel deletions of the PHOX2B gene.
Academic Article
Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.
Academic Article
Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.
Academic Article
Preferential beta-hexosaminidase (Hex) A (alpha beta) formation in the absence of beta-Hex B (beta beta) due to heterozygous point mutations present in beta-Hex beta-chain alleles of a motor neuron disease patient.
Academic Article
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.
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