Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome

This publication has 57 references indexed in Scilit:

• Identification of ataxia telangiectasia heterozygotes by flow cytometric analysis of X-ray damage
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1989
• Bloom's syndrome. XIV. The disorder in Japan
  Clinical Genetics, 1989
• Bloom's Syndrome. XII. Report from the Registry for 1987
  Clinical Genetics, 1989
• Breast and Other Cancers in Families with Ataxia-Telangiectasia
  New England Journal of Medicine, 1987
• G2 chromosomal radiosensitivity in ataxia telangiectasia lymphocytes
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1985
• Effects of X-irradiation on cell-cycle progression, induction of chromosomal aberrations and cell killing in ataxia telangiectasia (AT) fibroblasts
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1985
• Host-cell reactivation of UV-irradiated and chemically-treated herpes simplex virus-1 by xeroderma pigmentosum, XP heterozygotes and normal skin fibroblasts
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1978
• Bloom's syndrome in two Dutch families
  Clinical Genetics, 1977
• UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes
  Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1973
• Diabetes Mellitus and the Gene for Fanconi's Anemia
  Science, 1972