Ataxia-pancytopenia: Syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia

Cancer Genetics and Cytogenetics

Volumn 4, Issue 3, 1981, Pages 189-196

  Li, Frederick P ^a,b,c,d   Hecht, Frederick ^a,b,c,d   Kaiser McCaw, Barbara ^a,b,c,d   Baranko, Paul V ^a,b,c,d   Upp Potter, Nancy ^a,b,c,d  

^a NATIONAL CANCER INSTITUTE   (United States)

^b DANA FARBER CANCER INSTITUTE   (United States)

^c Southwest Biomedical Research Institute   (United States)

^d ST JOSEPH'S HOSPITAL AND MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE MYELOBLASTIC LEUKEMIA; APLASTIC ANEMIA; ATAXIA; BLOOD AND HEMOPOIETIC SYSTEM; CENTRAL NERVOUS SYSTEM; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; HEREDITY; IN VITRO STUDY; MONOSOMY 7; PANCYTOPENIA; PEDIGREE;

ADULT; ANEMIA, APLASTIC; ANEUPLOIDY; CEREBELLAR ATAXIA; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, 6-12 AND X; FEMALE; HUMANS; LEUKEMIA, MYELOCYTIC, ACUTE; LYMPHOCYTE ACTIVATION; MALE; PANCYTOPENIA; SYNDROME;

ATAXIA; RAPHIA FRATER;

EID: 0019784511     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(81)90013-3     Document Type: Article

References (25)

1. A family with acute leukemia, hypoplastic anemia and cerebellar ataxia
2. Genetic heterogeneity in xeroderma pigmentosum: Complementation groups and their relationship to DNA repair rates
3. Studies on repair of adenovirus 2 by human fibroblasts using normal, xeroderma pigmentosum, and xeroderma pigmentosum heterozygous strains
4. A simple cytogenetic test for increased mutagenic sensitivity
5. Chromosome instability syndromes
6. Somatic rearrangement of chromosome 14 in human lymphocytes
7. Acute myeloid leukaemia with monosomy-7 follows acute lymphoblastic leukemia
8. Pre-leukemia in children with a missing bone marrow C chromosome and a myeloproliferative disorder
9. Refractory anemia, granulocytic hyperplasia of bone marrow, and a missing chromosome in marrow cells. A new clinical syndrome?
10. C-monosomy myeloproliferative syndrome: A case of 7-monosomy
11. Myelofibrosis with C monosomy of marrow elements in a child
12. Two autopsy cases of atypical myeloproliferative disorder with group C monosomy occurring in siblings
13. Myeloproliferative disease in a child with monosomia of a C group chromosome
14. Fehlendes chromosom nr. 7 in der praleukemischen phase einer myeloblastenleukose bei einem kind
15. Chronic erythroleukemia with chromosome mosaicism—Report of a case in a 5-year old boy
16. A missing group C chromosome in the bone marrow cells of three children with myeloproliferative disease
17. Cell proliferation in the “preleukaemic” phase of acute leukemia—A cytophotometric and autoradiographic study
18. Chromosomal banding patterns in acute nonlymphocytic leukemia
19. Monosomy 7 in erythroleukaemia
20. Monosomy 7 in two patients with a myeloproliferative disorder
21. Chromosomal studies in preleukemia-I. Aneuploidy of group C chromosomes in three patients
22. Defective chemotaxis in monosomy-7
23. Immunodeficiency and the pathogenesis of non-Hodgkin's lymphoma
24. X-ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders