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Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.

作者信息

Shahid M J, Khouri F P, Ballas S K

出版信息

J Med Genet. 1972 Dec;9(4):474-8. doi: 10.1136/jmg.9.4.474.

DOI:10.1136/jmg.9.4.474
PMID:4646560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1469066/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/f94fda6db356/jmedgene00363-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/cabb4bec754f/jmedgene00363-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/fa3253dc7a6d/jmedgene00363-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/f94fda6db356/jmedgene00363-0096-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/cabb4bec754f/jmedgene00363-0094-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/fa3253dc7a6d/jmedgene00363-0095-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db54/1469066/f94fda6db356/jmedgene00363-0096-a.jpg

相似文献

1
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.
2
Bone marrow chromosomes in Fanconi's anaemia.范可尼贫血中的骨髓染色体
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Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution.范可尼贫血的细胞遗传学研究。一例伴有骨髓克隆进化病例的描述。
Clin Genet. 1974 Jan;5(1):72-6. doi: 10.1111/j.1399-0004.1974.tb01663.x.
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Nonrandom distribution of chromosome breaks in Fanconi's anemia.范科尼贫血中染色体断裂的非随机分布。
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[Chromosome abnormalities in bone marrow cells and peripheral lymphocytes in a patient with Fanconi's anemia].[范可尼贫血患者骨髓细胞和外周淋巴细胞中的染色体异常]
Minerva Med. 1981 Sep 22;72(35):2361-5.
6
[Chromosome aberrations in Fanconi's aplastic anemia].
Pediatr Pol. 1985 Jan;60(1):87-9.
7
[Fanconi's anemia: chromosome anormalies].
Sem Hop. 1976 Dec;52(44):2505-12.
8
[Somatic segregation and Fanconi's anemia].
C R Acad Hebd Seances Acad Sci D. 1975 Jul 28;281(4):297-300.
9
Fanconi's anaemia.
Q J Med. 1973 Apr;42(166):403-22.
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[Cytogenetic studies in four cases of Fanconi's anemia (author's transl)].
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引用本文的文献

1
Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia.烷化剂诱导范可尼贫血患者的姐妹染色单体交换和染色单体断裂
Proc Natl Acad Sci U S A. 1975 Oct;72(10):4066-70. doi: 10.1073/pnas.72.10.4066.
2
Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia.
Blut. 1977 Feb;34(2):119-32. doi: 10.1007/BF00999858.

本文引用的文献

1
Chromosome preparations of bone marrow cells without prior in vitro culture or in vivo colchicine administration.未经预先体外培养或体内给予秋水仙碱的骨髓细胞染色体标本制备。
Stain Technol. 1962 Jan;37:17-20. doi: 10.3109/10520296209114563.
2
Chromosome preparations of leukocytes cultured from human peripheral blood.从人外周血培养的白细胞的染色体标本制备。
Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.
3
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.
4
Panmyelopathy with congenital anomalies (Fanconi) in two cousins.
Helv Paediatr Acta. 1966 Jul;21(3):230-8.
5
Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues.范科尼贫血。多种组织中对染色体断裂的遗传性易感性。
Ann Intern Med. 1966 Sep;65(3):496-503. doi: 10.7326/0003-4819-65-3-496.
6
Chromosome abnormalities in constitutional aplastic anemia.先天性再生障碍性贫血中的染色体异常
N Engl J Med. 1966 Jan 6;274(1):8-14. doi: 10.1056/NEJM196601062740102.
7
Chromosomal aberrations and abnormalities of red-cell metabolism in a case of Fanconi's anaemia before and after development of leukaemia.范可尼贫血患者白血病发生前后的染色体畸变及红细胞代谢异常
Ger Med Mon. 1968 Mar;13(3):105-11.
8
Cytogenetical and clinical investigations in aplastic anaemia (Fancomi's type).
Humangenetik. 1971;13(3):222-33. doi: 10.1007/BF00326946.
9
Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies.
Blood. 1970 Sep;36(3):341-52.
10
Chromosomal aberrations in two cases of inherited aplastic anemia with unusual clinical features.两例具有不寻常临床特征的遗传性再生障碍性贫血中的染色体畸变
Ann Intern Med. 1969 Jul;71(1):107-17. doi: 10.7326/0003-4819-71-1-107.