Cancer in relatives of patients with aplastic anemia

Cancer Genetics and Cytogenetics

Volumn 9, Issue 1, 1983, Pages 61-65

  Potter, Nancy Upp ^a,b   Sarmousakis, Connie ^a,b   Li, Frederick P ^a,b  

^a NATIONAL CANCER INSTITUTE   (United States)

^b DANA FARBER CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APLASTIC ANEMIA; BLOOD AND HEMOPOIETIC SYSTEM; CANCER GENETICS; CANCER RISK; CLINICAL ARTICLE; ETIOLOGY; FANCONI ANEMIA; HEREDITY; HETEROZYGOTE; HUMAN; RELATIONSHIP;

ANEMIA, APLASTIC; FEMALE; HUMAN; MALE; NEOPLASMS; RISK; SUPPORT, NON-U.S. GOV'T;

EID: 0020619203     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(83)90025-0     Document Type: Article

References (16)

1. The bone marrow failure syndromes
2. Fanconi's anemia in the genetics of neoplasia
3. Reassessment of cancer predisposition of Fanconi anemia heterozygotes
4. Classification and aetiology of the aplastic anaemias
5. Third National Cancer Survey: Incidence data
6. Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method
7. The WT syndrome—A “new” autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia
8. Classical Fanconi anemia in a family with hypoplastic anemia
9. Ataxia-pancytopenia: Syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia
10. Syndrome of Shwachman and leukaemia
11. Variable phenotypic expression of an X-linked recessive lymphoproliferative syndrome
12. Dyskeratosis congenita: Clinical features and genetic aspects
13. Cancer in families with xeroderma pigmentosum
14. Malignant neoplasms in the families of patients with ataxia-telangiectasia
15. Cutaneous manifestations of ataxia-telangiectasia
16. Evaluation of mortality and cancer prevalence among Wiskott-Aldrich syndrome carrier females and selected intrafamilial controls