Fanconi Anemia: Clinical, Cytogenetic, and Experimental Aspects
Fanconi Anemia: Clinical, Cytogenetic, and Experimental Aspects
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范可尼贫血：临床、细胞遗传学和实验方面
DOI：
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发表时间：
1989
期刊：
影响因子：
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通讯作者：
G. Obe
中科院分区：
文献类型：
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作者：
T. Schroeder;A. Auerbach;G. Obe
I临床和治疗方面。国际范可尼贫血登记：第一次报告。范可尼贫血在荷兰。南非42例范可尼贫血患者的临床表现范可尼贫血的治疗方面。骨髓移植治疗范可尼贫血自发和诱导染色体断裂用于诊断范可尼贫血患者及其亲属。二环氧丁烷试验用于范可尼贫血的产前和产后诊断在诊断范可尼贫血时对交联剂反应的染色体断裂。范可尼贫血的细胞遗传学研究：诱发的染色体断裂和白血病的细胞遗传学。再生障碍性贫血和范可尼贫血：淋巴细胞对X线和丝裂霉素C的反应范可尼贫血患者、非范可尼贫血患者、其父母和子女以及对照先证者之间细胞敏感性的变化范可尼贫血患者父母细胞敏感性的意义范可尼贫血杂合子的染色体研究III范可尼贫血细胞缺陷的研究。BrdU-Hoechst流式细胞术将范可尼贫血的细胞动力学缺陷与氧超敏性联系起来。范可尼贫血的氧代谢和染色体断裂范可尼贫血基因的细胞效应及其显微注射校正范可尼贫血的表型和遗传异质性，交联的命运，以及通过DNA转染纠正缺陷。IV范可尼贫血的互补研究。范可尼贫血的互补研究范可尼贫血的互补和基因转移研究使用细胞融合和mRNA显微注射进行范科尼贫血的互补研究。-范可尼贫血：家庭的观点。范可尼贫血：家庭的观点。
I Clinical and Therapeutical Aspects.- International Fanconi Anemia Registry: First Report.- Fanconi Anemia in The Netherlands.- Clinical Aspects of a Cluster of 42 Patients in South Africa with Fanconi Anemia.- Therapeutic Aspects of Fanconi Anemia.- Bone Marrow Transplantation for Fanconi Anemia.- II Spontaneous and Induced Chromosomal Breakage for Diagnosis of Patients with Fanconi Anemia and Their Relatives.- Diepoxybutane Test for Prenatal and Postnatal Diagnosis of Fanconi Anemia.- Chromosomal Breakage in Response to Cross-linking Agents in the Diagnosis of Fanconi Anemia.- Cytogenetic Studies in Fanconi Anemia: Induced Chromosomal Breakage and Cytogenetics of Leukemia.- Aplastic Anemia and Fanconi Anemia: Response of Lymphocytes to X-Rays and Mitomycin C.- Variation in Cellular Sensitivities Among Fanconi Anemia Patients, Non-Fanconi Anemia-Patients, Their Parents and Siblings, and Control Probands.- Significance of Cellular Sensitivity in a Group of Parents of Fanconi Anemia Patients.- Chromosomal Studies in Fanconi Anemia Heterozygotes.- III Investigations of the Defect in Fanconi Anemia Cells.- BrdU-Hoechst Flow Cytometry Links the Cell Kinetic Defect of Fanconi Anemia to Oxygen Hypersensitivity.- Oxygen Metabolism and Chromosomal Breakage in Fanconi Anemia.- Cellular Effects of Fanconi Anemia Genes and Their Correction by Microinjection.- Phenotypic and Genetic Heterogeneity in Fanconi Anemia, Fate of Cross-Links, and Correction of the Defect by DNA Transfection.- IV Complementation Studies in Fanconi Anemia.- Complementation Studies in Fanconi Anemia.- Complementation and Gene Transfer Studies in Fanconi Anemia.- Complementation Studies in Fanconi Anemia Using Cell Fusion and Microinjection of mRNA.- V Fanconi Anemia: The Family's Point of View.- Fanconi Anemia: The Family's Point of View.