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[Familial neuroblastoma: cytogenetic investigation of the peripheral blood (author's transl)].

作者信息

Klein H, Plöchl E, Lampert F

出版信息

Humangenetik. 1975 Jul 23;28(3):217-20. doi: 10.1007/BF00278547.

DOI:10.1007/BF00278547
PMID:1150281
Abstract

A cytogenetic investigation was performed in a family which included 2 individuals with congenital neuroblastomas of the suprarenal gland confirmed by autopsy and one with a ganglioneuroblastoma of the thoracic wall as well as 3 other individuals with tumors which probably were also neuroblastomas. The lymphocytes of the peripheral blood of 5 healthy relatives as well as of the child with the treated ganglioneuroblastoma failed to show a constant alteration of chromosomes. In this family, therefore, the suggestion could not be proofed that the very rare familial aggregation of neuroblastomas is caused by a hereditary chromosomal aberration.

摘要

相似文献

1
[Familial neuroblastoma: cytogenetic investigation of the peripheral blood (author's transl)].
Humangenetik. 1975 Jul 23;28(3):217-20. doi: 10.1007/BF00278547.
2
[Familial neuroblastoma of the suprarenal glands in the newborn (author's transl)].新生儿肾上腺家族性神经母细胞瘤(作者译)
MMW Munch Med Wochenschr. 1974 Jun 7;116(23):1163-8.
3
Familial neuroblastoma.家族性神经母细胞瘤
J Pediatr. 1975 Nov;87(5):763-5. doi: 10.1016/s0022-3476(75)80304-0.
4
Chromosome findings and prognosis in 15 patients with neuroblastoma found by VMA mass screening.通过香草扁桃酸大规模筛查发现的15例神经母细胞瘤患者的染色体检查结果及预后
J Pediatr. 1988 Apr;112(4):567-71. doi: 10.1016/s0022-3476(88)80168-9.
5
Familial neuroblastoma: report of a kindred with a high incidence of infantile tumors.家族性神经母细胞瘤:一个婴儿期肿瘤高发家系的报告。
J Pediatr. 1972 Jan;80(1):74-7. doi: 10.1016/s0022-3476(72)80456-6.
6
Adrenal ganglioneuroma: a familial case.肾上腺神经节细胞瘤:1例家族性病例。
Urology. 2000 Sep 1;56(3):508. doi: 10.1016/s0090-4295(00)00695-6.
7
Familial neural crest tumours.家族性神经嵴肿瘤
Eur J Pediatr. 1991 Sep;150(11):789-92. doi: 10.1007/BF02026713.
8
Expression of folate sensitive and aphidicolin induced chromosomal fragile sites in familial neuroblastoma.家族性神经母细胞瘤中叶酸敏感性和阿非科林诱导的染色体脆性位点的表达
J Exp Clin Cancer Res. 2002 Sep;21(3):383-8.
9
Low occurrence of familial neuroblastomas and ganglioneuromas in five consecutive GPOH neuroblastoma treatment studies.在五项连续的德国儿童肿瘤学协会(GPOH)神经母细胞瘤治疗研究中,家族性神经母细胞瘤和神经节神经瘤的发生率较低。
Eur J Cancer. 2004 Dec;40(18):2760-5. doi: 10.1016/j.ejca.2004.08.007.
10
Association of cytogenetic abnormalities in a neuroblastoma and fragile sites expression.神经母细胞瘤中细胞遗传学异常与脆性位点表达的关联。
Br J Cancer. 1988 Sep;58(3):287-91. doi: 10.1038/bjc.1988.205.

本文引用的文献

1
[Ganglioneuroblastoma as hereditary disease of the sympathetic nervous system].[神经节神经母细胞瘤作为交感神经系统的遗传性疾病]
Beitr Pathol Anat. 1951;3(3):355-72.
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MINUTE CHROMATIN BODIES IN MALIGNANT TUMOURS OF CHILDHOOD.儿童恶性肿瘤中的微小染色质体
Lancet. 1965 Jul 10;1(7402):55-8. doi: 10.1016/s0140-6736(65)90131-5.
3
THE CHROMOSOMAL COMPLEMENT OF HUMAN SOLID TUMORS. II. KARYOTYPES OF GLIAL TUMORS.人类实体瘤的染色体组成。II. 神经胶质瘤的核型
J Neurosurg. 1965 Feb;22:160-8. doi: 10.3171/jns.1965.22.2.0160.
4
[Congenital embryonal neuroblastoma of the left adrenal gland].[左肾上腺先天性胚胎性神经母细胞瘤]
Munch Med Wochenschr. 1968 Feb 9;110(6):333-7.
5
Chromosomes of a human neuroblastoma: a new case with accessory minute chromosomes.一名人类神经母细胞瘤的染色体:一例伴有额外微小染色体的新病例。
J Natl Cancer Inst. 1968 Dec;41(6):1377-87.
6
Cytogenetic observations in children with neuroblastoma.神经母细胞瘤患儿的细胞遗传学观察
Pediatrics. 1971 May;47(5):839-43.
7
The identification of lymphocyte clones, with chromosome structural aberrations, in irradiated men and women.在接受辐射的男性和女性中识别出具有染色体结构畸变的淋巴细胞克隆。
Int J Radiat Biol Relat Stud Phys Chem Med. 1967;13(2):155-69. doi: 10.1080/09553006814550051.
8
Familial neuroblastoma.家族性神经母细胞瘤
Am J Dis Child. 1971 May;121(5):415-6. doi: 10.1001/archpedi.1971.02100160085010.
9
[Mechanisms and dynamics of chromosome aberrations in tumors. I. Introduction].[肿瘤中染色体畸变的机制与动力学。I. 引言]
Med Welt. 1972 Sep 16;23(38):1284-6.
10
Chromosomes and causation of human cancer and leukemia. 8. DMS chromosomes in a neuroblastoma.染色体与人类癌症及白血病的病因。8. 神经母细胞瘤中的双微体染色体。
Cancer. 1972 Jun;29(6):1671-9. doi: 10.1002/1097-0142(197206)29:6<1671::aid-cncr2820290635>3.0.co;2-c.