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J R Soc Med. 1989 September; 82(9): 555–556.
PMCID: PMC1292306

Anderson-Fabry disease: an unusual presentation with lymphadenopathy.

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Selected References

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  • Wallace HJ. Anderson-Fabry disease. Br J Dermatol. 1973 Jan;88(1):1–23. [PubMed]
  • Spence MW, Goldbloom AL, Burgess JK, D'entremont D, Ripley BA, Weldon KL. Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles. J Med Genet. 1977 Apr;14(2):91–99. [PMC free article] [PubMed]
  • Kleijer WJ, Hussaarts-Odijk LM, Sachs ES, Jahoda MG, Niermeijer MF. Prenatal diagnosis of Fabry's disease by direct analysis of chorionic villi. Prenat Diagn. 1987 May;7(4):283–287. [PubMed]
  • Morgan SH, Cheshire JK, Wilson TM, MacDermot K, Crawfurd MA. Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes. Pediatr Nephrol. 1987 Jul;1(3):536–539. [PubMed]
  • MacDermot KD, Morgan SH, Cheshire JK, Wilson TM. Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88. Hum Genet. 1987 Nov;77(3):263–266. [PubMed]
  • Bishop DF, Calhoun DH, Bernstein HS, Hantzopoulos P, Quinn M, Desnick RJ. Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme. Proc Natl Acad Sci U S A. 1986 Jul;83(13):4859–4863. [PubMed]
  • Morgan SH, Crawfurd MA. Anderson-Fabry disease. BMJ. 1988 Oct 8;297(6653):872–873. [PMC free article] [PubMed]

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