Triplication of 1q in Fanconi anemia

Cancer Genetics and Cytogenetics

Volumn 127, Issue 1, 2001, Pages 38-41

  Ferro, M Teresa ^a   Vazquez Mazariego, Yolanda ^a   Ramiro, Soraya ^a   Sanchez Hombre, M Carmen ^a   Villalon, Concepcion ^a   Garcia Sagredo, Jose M ^a   Ulibarrena, Carlos ^b   Sastre, Jose L ^b   Roman, Carlos San ^a  

^a HOSPITAL RAMÓN Y CAJAL   (Spain)

^b Complejo Hospitalario Cristal Pior ^*  (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CANCER GENETICS; CASE REPORT; CHROMOSOME 1; CHROMOSOME 1Q; CHROMOSOME 3; CHROMOSOME ABERRATION; CHROMOSOME BREAKAGE; CYTOGENETICS; FANCONI ANEMIA; HUMAN; MALE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

ADULT; BONE MARROW; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; CYTOGENETIC ANALYSIS; FANCONI ANEMIA; HUMANS; MALE; SISTER CHROMATID EXCHANGE;

EID: 0035335092     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(00)00415-5     Document Type: Article

References (7)

1. Fanconi anemia and bone marrow clonal chromosome abnormalities
2. Fanconi anemia; myelodysplasia as a predictor of outcome
3. Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1q12-32 triplication) via BrdU/Hoechst flow cytometry
4. Chromosome abnormalities in bone marrow of Fanconi anemia patients
5. Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry
6. Cytogenetic findings in a Fanconi anemia patient with AML
7. Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literatuer