Hla in familial hodgkin's disease. Results and a new hypothesis

International Journal of Cancer

Volumn 19, Issue 4, 1977, Pages 450-455

  Marshall, William H ^a   Barnard, John M ^a   Buehler, Sharon K ^a   Crumley, Joyce ^a   Larsen, Bodil ^a  

^a MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT DEFICIENCY; GENETICS; HLA SYSTEM; HODGKIN DISEASE; IMMUNOGENETICS; IN VITRO STUDY; MAJOR CLINICAL STUDY; NORMAL HUMAN;

ANTIGENS, NEOPLASM; FEMALE; GENE FREQUENCY; HAPLOIDY; HISTOCOMPATIBILITY ANTIGENS; HISTOCOMPATIBILITY TESTING; HLA ANTIGENS; HODGKIN DISEASE; HUMANS; MALE; NEWFOUNDLAND; PEDIGREE;

EID: 0017340603     PISSN: 00207136     EISSN: 10970215     Source Type: Journal    
DOI: 10.1002/ijc.2910190403     Document Type: Article

References (6)

1. Discussion of association between HL‐A type and specific disease entities
2. Common variable immunodeficiency, Hodgkin's disease and other malignancies in a Newfoundland family
3. LD‐7a association with C2 deficiency in five of six families.
4. HLA haplotypes in a genetic isolate in Newfoundland. A population showing 8% homozygosity and a familial aggregate of lymphoma and immunodeficiency cases
5. HL‐A and disease association—A survey
6. Epidemiology of Hodgkin's disease: review and etiological leads