Fanconi Anemia
- 1 March 2000
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 117 (2) , 125-131
- https://doi.org/10.1016/s0165-4608(99)00159-4
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Detection of Monosomy 7 in Bone Marrow by Fluorescence In Situ HybridizationCancer Genetics and Cytogenetics, 1999
- Double Esterase Staining andOther Neutrophilic Granule Abnormalities in 237 Patients with the Myelodysplastic Syndrome Studied by the Cancer and Leukemia Group BActa Haematologica, 1998
- Evidence for at Least Eight Fanconi Anemia GenesAmerican Journal of Human Genetics, 1997
- Deficiency of neutrophilic granule membrane glycoproteins in the myelodysplastic syndromes: A common deficiency in 216 patients studied by the cancer and leukemia group BLeukemia Research, 1997
- Induction of a hematological and cytogenetic remission in a patient with a myelodysplastic syndrome secondary to Fanconi's anemia employing the S-HAM regimenAnnals of Hematology, 1997
- Fanconi's anemia and malignanciesAmerican Journal of Hematology, 1996
- Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia: a pilot studyBlood, 1996
- Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study [see comments]Blood, 1994
- Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?British Journal of Haematology, 1993
- Proposals for the classification of the myelodysplastic syndromesBritish Journal of Haematology, 1982