Genetics of Neoplasia--impact of Ecogenetics on Oncogenesis. A Review

Overview

Journal Am J Pathol

Publisher Elsevier

Specialty Pathology

Date 1978 Jun 1

PMID 207190

Citations 4

Authors

D T Purtilo

L Paquin

T Gindhart

Affiliations

Soon will be listed here.

Citing Articles

Turcot's syndrome and familial adenomatous polyposis associated with brain tumor: review of related literature.

Itoh H, Hirata K, Ohsato K Int J Colorectal Dis. 1993; 8(2):87-94.

PMID: 8409693 DOI: 10.1007/BF00299334.

Increased prevalence of minor anomalies in childhood malignancy.

Mehes K, Signer E, Pluss H, Muller H, Stalder G Eur J Pediatr. 1985; 144(3):243-54.

PMID: 4054163 DOI: 10.1007/BF00451951.

Familial glioma: occurrence within the "familial cancer syndrome" and systemic malformations.

Vieregge P, Gerhard L, Nahser H J Neurol. 1987; 234(4):220-32.

PMID: 3612193 DOI: 10.1007/BF00618254.

Glioblastoma multiforme in three family members, including a case of true multicentricity.

Heuch I, Blom G J Neurol. 1986; 233(3):142-4.

PMID: 3014072 DOI: 10.1007/BF00314419.

References

Kopelovich L, Pfeffer L, Lipkin M . Recent studies on the identification of proliferative abnormalities and of oncogenic potential of cutaneous cells in individuals at increased risk of colon cancer. Semin Oncol. 1976; 3(4):369-72. View

Aiuti F, BUSINCO L, Griscelli C, TOURAINE J, Webster A . Improvements in methods for identifying patients with severe combined immunodeficiency and related syndromes. Z Immunitatsforsch Immunobiol. 1977; 153(2):95-106. View

Purtilo D . Opportunistic non-Hodgkin's lymphoma in X-linked recessive immunodeficiency and lymphoproliferative syndromes. Semin Oncol. 1977; 4(3):335-43. View

Dausset J, Hors J . Some contributions of the HL-A complex to the genetics of human diseases. Transplant Rev. 1975; 22:44-74. DOI: 10.1111/j.1600-065x.1975.tb01551.x. View

Aiuti F, Rocchi G, DAmelio R, Giunta S, Fiorilli M . Lymphoid cells in infectious mononucleosis classified according to T and B cell markers. Int Arch Allergy Appl Immunol. 1975; 48(3):353-63. DOI: 10.1159/000231320. View

Buehler S, Firme F, Fodor G, Fraser G, Marshall W, Vaze P . Common variable immunodeficiency, Hodgkin's disease, and other malignancies in a Newfoundland family. Lancet. 1975; 1(7900):195-7. DOI: 10.1016/s0140-6736(75)91361-6. View

Purtilo D, Cassel C, Yang J, Harper R . X-linked recessive progressive combined variable immunodeficiency (Duncan's disease). Lancet. 1975; 1(7913):935-40. DOI: 10.1016/s0140-6736(75)92004-8. View

Doherty P, Zinkernagel R . A biological role for the major histocompatibility antigens. Lancet. 1975; 1(7922):1406-9. DOI: 10.1016/s0140-6736(75)92610-0. View

Pendergrass T, Mann D, Stoller R, Halterman R, Fraumeni Jr J . Acute myelocytic leukaemia and leukaemia-associated antigens in sisters. Lancet. 1975; 2(7932):429-31. DOI: 10.1016/s0140-6736(75)90844-2. View

10.

Everson R, Li F, Fraumeni Jr J, Fishman J, Wilson R, Stout D . Familial male breast cancer. Lancet. 1976; 1(7949):9-12. DOI: 10.1016/s0140-6736(76)92907-x. View

11.

Klein G, Svedmyr E, Jondal M, PERSSON P . EBV-determined nuclear antigen (EBNA)-positive cells in the peripheral blood of infectious mononucleosis patients. Int J Cancer. 1976; 17(1):21-6. DOI: 10.1002/ijc.2910170105. View

12.

Tauber J . "Self": standard of comparison for immunological recognition of foreignness. Lancet. 1976; 2(7980):291-3. DOI: 10.1016/s0140-6736(76)90737-6. View

13.

Purtilo D . Pathogenesis and phenotypes of an X-linked recessive lymphoproliferative syndrome. Lancet. 1976; 2(7991):882-5. DOI: 10.1016/s0140-6736(76)90542-0. View

14.

Hirschhorn K . Chromosomes and cancer. Birth Defects Orig Artic Ser. 1976; 12(1):113-21. View

15.

Cunningham A . Lymphomas and animal-protein consumption. Lancet. 1976; 2(7996):1184-6. DOI: 10.1016/s0140-6736(76)91694-9. View

16.

Coovadia H, Wesley A, Brain P, Henderson L, Hallett A, Vos G . Immunoparesis and outcome in measles. Lancet. 1977; 1(8012):619-21. DOI: 10.1016/s0140-6736(77)92056-6. View

17.

Frichot 3rd B, Lynch H, Guirgis H, Harris R, Lynch J . New cutaneous phenotype in familial malignant melanoma. Lancet. 1977; 1(8016):864-5. DOI: 10.1016/s0140-6736(77)92822-7. View

18.

Dutrillaux B, Couturier J, Viegas-Pequignot E, Schaison G . Localization chromatid breaks in Fanconi's anemia, using three consecutive stains. Hum Genet. 1977; 37(1):65-71. DOI: 10.1007/BF00293773. View

19.

Tragl K, Mayr W . Familial islet-cell adenomatosis. Lancet. 1977; 2(8035):426-8. DOI: 10.1016/s0140-6736(77)90609-2. View

20.

Lynch H, Guirgis H, Harris R . Familial susceptibility to lung cancer and chronic obstructive pulmonary disease. Lancet. 1977; 2(8042):815. DOI: 10.1016/s0140-6736(77)90740-1. View