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8. Familial spontaneous pneumothorax-report of seven cases in two families. Cheng YJ; Chou SH; Kao EL Gaoxiong Yi Xue Ke Xue Za Zhi; 1992 Jul; 8(7):390-4. PubMed ID: 1433444 [TBL] [Abstract][Full Text] [Related]
9. Familial spontaneous pneumothorax in three generations and its HLA. Yamada A; Takeda Y; Hayashi S; Shimizu K Jpn J Thorac Cardiovasc Surg; 2003 Sep; 51(9):456-8. PubMed ID: 14529166 [TBL] [Abstract][Full Text] [Related]
10. Family occurrence and hla system in tumoral calcinosis. Todesco S; Venturi Pasini C; Glorioso S; Fagiolo U Int Surg; 1983; 68(1):89-90. PubMed ID: 6853092 [TBL] [Abstract][Full Text] [Related]
12. IgA nephropathy occurring in two siblings of three families. Kabasakal C; Keskinoğlu A; Mir S; Başdemir G Turk J Pediatr; 1997; 39(3):395-401. PubMed ID: 9339120 [TBL] [Abstract][Full Text] [Related]
13. HLA antigens in haemophilic arthritis: a family study. Steven MM; Sturrock RD; Forbes CD; Dick HM Dis Markers; 1986 Oct; 4(3):239-42. PubMed ID: 3452480 [TBL] [Abstract][Full Text] [Related]
14. Primary spontaneous pneumothorax in two siblings suggests autosomal recessive inheritance. Koivisto PA; Mustonen A Chest; 2001 May; 119(5):1610-2. PubMed ID: 11348979 [TBL] [Abstract][Full Text] [Related]
15. HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus. Braathen LR; Bratlie A; Teisberg P Acta Derm Venereol; 1986; 66(5):419-22. PubMed ID: 2431580 [TBL] [Abstract][Full Text] [Related]
16. HLA antigens in patients with Heberden's nodes. Tomer Y; Zamir R; Brautbar C; Pinkhas J; Weinberger A Isr J Med Sci; 1988 Jan; 24(1):24-7. PubMed ID: 3346145 [TBL] [Abstract][Full Text] [Related]
17. Possible association of specific HLA haplotype in a pedigree with familial polyposis coli. Nagatomo Y; Yoshida T; Kodama K; Kambe H; Tanaka K Am J Gastroenterol; 1987 Sep; 82(9):910-1. PubMed ID: 2820223 [TBL] [Abstract][Full Text] [Related]
18. [Hypertrophic cardiomyopathy occurring in the family. Rare coexistence with oligophrenia. Clinical examinations, cytogenetic and HLA system]. Krzymińska E; Szczerkowska Z; Linom J; Swiatecka G; Pawlak T; Maniszewska B; Luberda Z Kardiol Pol; 1993 Aug; 39(8):84-9; discussion 90. PubMed ID: 8231010 [TBL] [Abstract][Full Text] [Related]
19. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system. Venneker GT; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; de Waall LP; Bos JD; Asghar SS Exp Clin Immunogenet; 1996; 13(2):104-11. PubMed ID: 9063702 [TBL] [Abstract][Full Text] [Related]