Familial Paroxysmal Polyserositis. Clinical and Laboratory Findings in 120 Cases
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Involvement of the modifier gene of a human Mendelian disorder in a negative selection process.
Jeru I, Hayrapetyan H, Duquesnoy P, Cochet E, Serre J, Feingold J PLoS One. 2009; 4(10):e7676.
PMID: 19888326 PMC: 2765618. DOI: 10.1371/journal.pone.0007676.
Familial Mediterranean fever in Arab children: the high prevalence and gene frequency.
Rawashdeh M, Majeed H Eur J Pediatr. 1996; 155(7):540-4.
PMID: 8831074 DOI: 10.1007/BF01957901.
Autosomal recessive disorders among Arabs: an overview from Kuwait.
Teebi A J Med Genet. 1994; 31(3):224-33.
PMID: 8014972 PMC: 1049748. DOI: 10.1136/jmg.31.3.224.
Retroperitoneal lymphadenopathy in familial Mediterranean fever.
Rimon D, Meir Y, Cohen L Postgrad Med J. 1989; 65(768):776-8.
PMID: 2694140 PMC: 2429824. DOI: 10.1136/pgmj.65.768.776.
Familial Mediterranean fever (recurrent hereditary polyserositis) in children: analysis of 88 cases.
Majeed H, Barakat M Eur J Pediatr. 1989; 148(7):636-41.
PMID: 2663516 DOI: 10.1007/BF00441519.