Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1
2012 ◽
Vol 11
(3)
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pp. 215-217
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2006 ◽
Vol 21
(1)
◽
pp. 43
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2010 ◽
Vol 29
(4-6)
◽
pp. 509-514
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