Panmyelopathy with congenital anomalies (Fanconi) in two cousins.

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作者信息

Hoefnagel D, Sullivan M, McIntyre O R, Gray J A, Storrs R C

出版信息

Helv Paediatr Acta. 1966 Jul;21(3):230-8.

PMID:5990992

Abstract

摘要

相似文献

Panmyelopathy with congenital anomalies (Fanconi) in two cousins.

Helv Paediatr Acta. 1966 Jul;21(3):230-8.

[Aplasia of the thumbs and thrombocytopenia (Fanconi): a clinical, hematological and cytogenetic study of a patient and his family].[拇指发育不全与血小板减少症（范科尼贫血）：对一名患者及其家族的临床、血液学和细胞遗传学研究]

J Genet Hum. 1975 Oct;23 SUPPL:106.

Cytogenic observations in congenital familial panmyelopathy (Fanconi's syndrome).先天性家族性全骨髓病（范科尼综合征）的细胞遗传学观察

Nouv Rev Fr Hematol. 1971 Sep-Oct;11(5):781-90.

The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia.WT综合征——一种“新的”常染色体显性多效性性状，表现为桡骨/尺骨发育不全，伴有骨髓衰竭和/或白血病的高风险。

Birth Defects Orig Artic Ser. 1977;13(3B):31-8.

[Chromosome abnormalities in a case of Fanconi's syndrome].[范科尼综合征一例的染色体异常]

Nouv Rev Fr Hematol. 1970 Mar-Apr;10(2):266-9.

[Chromosome abnormalities in a case of Fancon's anemia].[范可尼贫血一例中的染色体异常]

Minerva Med. 1973 May 2;64(30):1633-7.

[Chromosal fragility in familial panmyelopathy (Fanconi type)].[家族性全骨髓病（范可尼型）中的染色体脆性]

Schweiz Med Wochenschr. 1965 Oct 23;95(43):1461-4.

Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome.范可尼型遗传性肾小管疾病和特发性范可尼综合征。

Prog Clin Biol Res. 1989;305:111-35.

[Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].

Humangenetik. 1966;2(3):287-316. doi: 10.1007/BF00395947.

[Spontaneous chromosome aberrations in familial panmyelopathy].[家族性全髓病中的自发染色体畸变]

Humangenetik. 1964;1(2):194-6. doi: 10.1007/BF00389636.

引用本文的文献

Clinical and chromosome studies in Fanconi's aplastic anaemia.范科尼贫血的临床与染色体研究

J Med Genet. 1969 Mar;6(1):28-33. doi: 10.1136/jmg.6.1.28.

Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.范科尼贫血的染色体特性及“体外”检查

Humangenetik. 1969;7(4):314-22. doi: 10.1007/BF00283553.

Cytogenetical and clinical investigations in aplastic anaemia (Fancomi's type).

Humangenetik. 1971;13(3):222-33. doi: 10.1007/BF00326946.

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.

Formal genetics of Fanconi's anemia.

Hum Genet. 1976 Jun 29;32(3):257-88. doi: 10.1007/BF00295817.

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