Diepoxybutane Test for Prenatal and Postnatal Diagnosis of Fanconi Anemia
- 1 January 1989
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- HLA typing used with cultured amniotic and chorionic villus cells for early prenatal diagnosis or parentage testing without one parent's availabilityHuman Immunology, 1986
- First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 cases.Journal of Medical Genetics, 1985
- Effect of procarbazine and cyclophosphamide on chromosome breakage in Fanconi anemia cells: Relevance to bone marrow transplantationCancer Genetics and Cytogenetics, 1983
- FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: THREE CASESThe Lancet, 1982
- Acute myeloid leukemia as the first hematologic manifestation of fanconi anemiaAmerican Journal of Hematology, 1982
- Absence of chromosome heterogeneity between classical Fanconi's anemia and the Estren-Dameshek typeCancer Genetics and Cytogenetics, 1980
- Nitrogen mustard-induced chromosome breakage: A tool for Fanconi's anemia diagnosisCancer Genetics and Cytogenetics, 1980
- Bone Marrow Transplantation in Fanconi AnaemiaBritish Journal of Haematology, 1980
- Specific cellular defects in patients with Fanconi anemiaJournal of Cellular Physiology, 1979
- Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogensNature, 1976