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Journal Abstract Search


144 related items for PubMed ID: 6303650

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  • 8. Heterozygote detection in Fabry's disease using mailed hair roots.
    Vermorken AJ, van Bennekom CA, de Bruyn CH, Oei TL, Frohlich J.
    Br J Dermatol; 1980 Jul; 103(1):101-3. PubMed ID: 6252938
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  • 9. Loss of electron-dense lamellar material from Fabry's disease fibroblasts after enzyme replacement.
    Sifers RN, Mayes JS, Nordquist RE.
    Hum Genet; 1983 Jul; 65(1):85-7. PubMed ID: 6315565
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  • 10. Clinical features and genetic analysis of a Chinese kindred with Fabry's disease.
    Tse KC, Chan KW, Tin VP, Yip PS, Tang S, Li FK, Ho YW, Lai KN, Chan TM.
    Nephrol Dial Transplant; 2003 Jan; 18(1):182-6. PubMed ID: 12480979
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  • 15. Identification of Fabry's disease by the screening of alpha-galactosidase A activity in male and female hemodialysis patients.
    Tanaka M, Ohashi T, Kobayashi M, Eto Y, Miyamura N, Nishida K, Araki E, Itoh K, Matsushita K, Hara M, Kuwahara K, Nakano T, Yasumoto N, Nonoguchi H, Tomita K.
    Clin Nephrol; 2005 Oct; 64(4):281-7. PubMed ID: 16240899
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