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Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia.

作者信息

Schmid W

出版信息

Semin Hematol. 1967 Jul;4(3):241-9.

PMID:6074579
Abstract
摘要

相似文献

1
Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). II. A discussion of the cytogenetic findings in Fanconi's anemia.
Semin Hematol. 1967 Jul;4(3):241-9.
2
Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects.家族性体质性全骨髓细胞病，范科尼贫血（F.A.）。I. 临床方面。
Semin Hematol. 1967 Jul;4(3):233-40.
3
Editorial: Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.).
J Assoc Physicians India. 1974 Jul;22(7):552-3.
4
Fibroblasts from patients with Fanconi's anemia are not deficient in excision of thymine dimer.范科尼贫血患者的成纤维细胞在切除胸腺嘧啶二聚体方面并不缺乏。
Eur J Cell Biol. 1985 May;37:240-2.
5
[Chromosome changes in Fanconi's anemia (FA) and clinical course of the disease (familial constitutional panmyelopathy)].
Pol Tyg Lek. 1972 Nov 6;27(45):1758-61.
6
[Fanconi's anemia type Estren-Dameshek. A case report (author's transl)].
Pediatr Med Chir. 1981 Nov-Dec;3(6):575-8.
7
Association of aplastic anaemia and Fanconi's disease with HLA-DRB1 alleles.再生障碍性贫血和范科尼贫血与HLA-DRB1等位基因的关联。
Int J Immunogenet. 2008 Dec;35(6):453-6. doi: 10.1111/j.1744-313X.2008.00810.x.
8
[Chromosome aberrations in Fanconi's aplastic anemia].
Pediatr Pol. 1985 Jan;60(1):87-9.
9
[Familial aplastic myelopathy (Fanconi's syndrome). Clinical contribution].
Atti Accad Fisiocrit Siena Med Fis. 1967;16(2):1447-69.
10
[Fanconi's congenital aplastic anemia in a 7-year-old child].
Pediatr Akus Ginekol. 1972;6:30.

引用本文的文献

1
Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts.通过与正常人成纤维细胞进行细胞融合抑制范科尼贫血中自发的和丝裂霉素C诱导的染色体畸变。
Hum Genet. 1980;55(2):223-6. doi: 10.1007/BF00291770.
2
Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.与细胞动力学相关的诱导性和自发性染色体畸变的频率及类型
Hum Genet. 1981;59(2):137-40. doi: 10.1007/BF00293063.
3
A case of pure red cell aplasia with a high incidence of spontaneous chromosome breakage: a possible X-ray sensitive syndrome.
一例伴有高发性自发染色体断裂的纯红细胞再生障碍性贫血：一种可能的X线敏感综合征。
Hum Genet. 1980;55(3):337-40. doi: 10.1007/BF00290214.
4
Cytogenetical and clinical investigations in aplastic anaemia (Fancomi's type).
Humangenetik. 1971;13(3):222-33. doi: 10.1007/BF00326946.
5
Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.范科尼贫血：1例骨髓细胞存在显著染色体异常患者的报告。
J Med Genet. 1972 Dec;9(4):474-8. doi: 10.1136/jmg.9.4.474.
6
Localization chromatid breaks in Fanconi's anemia, using three consecutive stains.
Hum Genet. 1977 Jun 10;37(1):65-71. doi: 10.1007/BF00293773.