A 46, XY, dup (1) (q21q32), add(11) (q23) karyotype in a case of Fanconi anemia

Leukemia Research

Volumn 25, Issue 4, 2001, Pages 347-348

  Babu Rao, V ^a   Kerketta, L ^a   Ghosh, K ^a   Mohanty, D ^a  

^a KEM HOSPITAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; FANCONI ANEMIA; HUMAN; KARYOTYPE; KARYOTYPE 46,XY; MALE; PRIORITY JOURNAL;

ADOLESCENT; BONE MARROW CELLS; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKAGE; CHROMOSOME FRAGILITY; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 11; CYTOGENETIC ANALYSIS; GENE DUPLICATION; HUMANS; KARYOTYPING; MALE;

EID: 0035119845     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(00)00113-2     Document Type: Article

References (8)

1. Fanconi anemia
2. Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi Anemia
3. Fanconi anaemia and leukaemia: tracking the genes
4. Leukemia and preleukemia in Fanconi anemia patients
5. Chromosome abnormalities in bone marrow of Fanconi anemia patients
6. Spontaneous chromosome aberrations in Fanconi anemia patients are located at fragile sites and acute myeloid leukemia break points
7. The Fanconi anaemia group G gene FANCG is identical with XRCC9
8. Amplification of the 11q23 region in acute myeloid leukemia