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J R Soc Med. 1991 July; 84(7): 438–439.
PMCID: PMC1293343

5 q-syndrome and monoclonal gammopathy with alpha 1 antitrypsin deficiency.

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Selected References

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  • Van den Berghe H, Vermaelen K, Mecucci C, Barbieri D, Tricot G. The 5q-anomaly. Cancer Genet Cytogenet. 1985 Jul;17(3):189–255. [PubMed]
  • Van den Berghe H. The 5q- syndrome. Scand J Haematol Suppl. 1986;45:78–81. [PubMed]
  • Dewald GW, Kyle RA, Hicks GA, Greipp PR. The clinical significance of cytogenetic studies in 100 patients with multiple myeloma, plasma cell leukemia, or amyloidosis. Blood. 1985 Aug;66(2):380–390. [PubMed]
  • Sokal G, Michaux JL, Van Den Berghe H, Cordier A, Rodhain J, Ferrant A, Moriau M, De Bruyere M, Sonnet J. A new hematologic syndrome with a distinct karyotype: the 5 q--chromosome. Blood. 1975 Oct;46(4):519–533. [PubMed]
  • Breit SN, Wakefield D, Robinson JP, Luckhurst E, Clark P, Penny R. The role of alpha 1-antitrypsin deficiency in the pathogenesis of immune disorders. Clin Immunol Immunopathol. 1985 Jun;35(3):363–380. [PubMed]
  • Szczeklik A, Stachura J, Pietoń R, Serwońska M. Marskoś watroby i dysimmunologlobulinemia u chorego z niedoborem alpha 1-antytrypsyny o fenotypie Pi M. Pol Arch Med Wewn. 1977 Jun;57(6):533–537. [PubMed]

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