一项家族性耳聋的细胞遗传学研究。 - Suppr

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超能文献

A cytogenetic study of familial deafness.

作者信息

Dar H, Winter S T

出版信息

J Med Genet. 1969 Sep;6(3):298-303. doi: 10.1136/jmg.6.3.298.

DOI:10.1136/jmg.6.3.298

PMID:5345103

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468737/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8277/1468737/b36dca18785a/jmedgene00374-0070-a.jpg

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本文引用的文献

ENDOREDUPLICATED CHROMOSOMES.

Lancet. 1965 May 29;1(7396):1169-70. doi: 10.1016/s0140-6736(65)92004-0.

CYTOGENETIC AND CLINICAL FINDINGS IN 48 PATIENTS WITH CONGENITALLY DEFECTIVE OR ABSENT OVARIES.48例先天性卵巢缺陷或缺失患者的细胞遗传学和临床研究结果

Medicine (Baltimore). 1965 Mar;44:135-64. doi: 10.1097/00005792-196503000-00002.

ENDOREDUPLICATION AND DISEASE.

Lancet. 1965 Apr 24;1(7391):915. doi: 10.1016/s0140-6736(65)92655-3.

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.

Recessive early-onset neural deafness.

Acta Otolaryngol. 1967 Oct;64(4):313-26. doi: 10.3109/00016486709139119.

Cytogenetic study of otosclerosis.

Acta Genet Med Gemellol (Roma). 1967 Apr;16(2):124-58. doi: 10.1017/s1120962300013159.

[Morphologic anomalies of the chromosomes of the 16th pair and the acoustic apparatus].

Acta Otolaryngol. 1967 Feb-Mar;63(2):144-8.

Chromosomal damage in human leukocytes induced by lysergic acid diethylamide.麦角酸二乙酰胺诱导的人白细胞染色体损伤。

Science. 1967 Mar 17;155(3768):1417-9. doi: 10.1126/science.155.3768.1417.

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.

Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth.先天性毛细血管扩张性红斑及生长发育迟缓中的染色体断裂与急性白血病。

Ann Intern Med. 1966 Sep;65(3):487-95. doi: 10.7326/0003-4819-65-3-487.

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