Genetic linkage studies in a Negro kindred with Norrie's disease.
作者信息
Nance W E, Hara S, Hansen A, Elliott J, Lewis M, Chown B
出版信息
Am J Hum Genet. 1969 Sep;21(5):423-9.
Abstract
摘要
相似文献
1
Genetic linkage studies in a Negro kindred with Norrie's disease.对一个患有诺里病的黑人家族进行的基因连锁研究。
Am J Hum Genet. 1969 Sep;21(5):423-9.
2
Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis.以色列人中X连锁鱼鳞病与Xg血型及X染色体其他标记物的连锁关系。
Ann Hum Genet. 1969 May;32(4):323-32. doi: 10.1111/j.1469-1809.1969.tb00082.x.
3
New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.X连锁型肌营养不良症、葡萄糖-6-磷酸脱氢酶（G6PD）变异体、色盲和Xg血型的新连锁数据。
J Med Genet. 1974 Dec;11(4):321-7. doi: 10.1136/jmg.11.4.321.
4
Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.美国黑人中葡萄糖-6-磷酸脱氢酶缺乏症基因座与色盲基因座之间的遗传连锁
Ann Hum Genet. 1962 Nov;26:107-22. doi: 10.1111/j.1469-1809.1962.tb01316.x.
5
Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.可能是由突变引起的诺里病。两个同胞兄弟的散发病例，每个家族中有两名男性，对其中一例进行了尸检，并结合诺里病计算了基因突变频率。
Br J Ophthalmol. 1986 Apr;70(4):305-13. doi: 10.1136/bjo.70.4.305.
6
Falciform fold, retinal detachment, and Norrie's disease.镰状皱襞、视网膜脱离与诺里病。
Am J Ophthalmol. 1980 Jul;90(1):76-80. doi: 10.1016/s0002-9394(14)75079-2.
7
[Heredity of congenital deficiencies in color vision].[先天性色觉缺陷的遗传]
Acta Genet Med Gemellol (Roma). 1972 Jul;21(3):233-56. doi: 10.1017/s1120962300010957.
8
Norrie's disease.诺里病
South Med J. 1971 Nov;64(11):1317-21. doi: 10.1097/00007611-197111000-00003.
9
Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.撒丁岛两个X连锁基因的连锁不平衡及其对人类X染色体统计定位的影响。
Genetics. 1977 May;86(1):199-212. doi: 10.1093/genetics/86.1.199.
10
Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.法裔加拿大人家族中的诺里病：通过DNA分析检测携带者的尝试。
Can J Ophthalmol. 1987 Feb;22(1):21-3.
引用本文的文献
1
A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.使用下一代测序技术的基因组流行病学研究的研究设计与统计方法综述。
Front Genet. 2015 Apr 20;6:149. doi: 10.3389/fgene.2015.00149. eCollection 2015.
2
Retinal dysplasia.视网膜发育异常
Doc Ophthalmol. 1981 Jul 15;51(3):277-88. doi: 10.1007/BF00143890.
3
Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.一名女性中类似诺里病的原发性玻璃体视网膜发育异常：与X-常染色体易位相关
Br J Ophthalmol. 1986 Jan;70(1):64-71. doi: 10.1136/bjo.70.1.64.
4
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.诺里病（一种来自近端短臂的克隆DNA序列）与X染色体着丝粒之间的紧密连锁。
Hum Genet. 1985;71(3):211-4. doi: 10.1007/BF00284575.
5
Norrie disease gene is distinct from the monoamine oxidase genes.诺里病基因与单胺氧化酶基因不同。
Am J Hum Genet. 1989 Sep;45(3):424-34.
6
Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.诺里病与X染色体鸟氨酸转氨酶的连锁分析。
Trans Am Ophthalmol Soc. 1992;90:405-79.
7
A presumptive new variant of Norrie's disease.诺里病的一种疑似新变体。
J Med Genet. 1979 Apr;16(2):125-8. doi: 10.1136/jmg.16.2.125.
本文引用的文献
1
Distribution of blood factors, ABO, MN and Rh in a group of American Negroes.一组美国黑人的血型因子（ABO、MN和Rh）分布情况。
Am J Phys Anthropol. 1955 Mar;13(1):121-8. doi: 10.1002/ajpa.1330130109.
2
NORRIE'S DISEASE AND THE XG BLOOD GROUP SYSTEM: LINKAGE DATA.
Acta Genet Stat Med. 1965;15:103-15. doi: 10.1159/000151898.
3
GENETIC AND BIOCHEMICAL CONSIDERATIONS OF THE SERUM GROUP-SPECIFIC COMPONENT.血清群特异性成分的遗传学和生物化学考量
Cold Spring Harb Symp Quant Biol. 1964;29:435-42. doi: 10.1101/sqb.1964.029.01.045.
4
Norie's disease (atrofia bulborum hereditaria).诺里病（遗传性眼球萎缩）。
Acta Ophthalmol (Copenh). 1963;41:134-46. doi: 10.1111/j.1755-3768.1963.tb03533.x.
5
The Henshaw blood factor in New York City Negroes.纽约市黑人中的亨肖血液因子。
Am J Phys Anthropol. 1956 Sep;14(3):445-7. doi: 10.1002/ajpa.1330140319.
6
Sequential tests for the detection of linkage.用于检测连锁的序贯检验。
Am J Hum Genet. 1955 Sep;7(3):277-318.
7
The incidence of multiple births in man and some of the other unipara.人类及其他一些单胎动物的多胎发生率。
Obstet Gynecol. 1953 Jul;2(1):22-35.
8
The linkage relation of Xg to g-6-pd in Israelis: the evidence of a second series of families.以色列人中Xg与葡萄糖-6-磷酸脱氢酶（g-6-pd）的连锁关系：第二批家系的证据。
Ann Hum Genet. 1967 Jan;30(3):211-8. doi: 10.1111/j.1469-1809.1967.tb00022.x.
9
Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration.
Acta Ophthalmol (Copenh). 1966:Suppl 89:1-47.
10
Norrie's disease.诺里病
Am J Ophthalmol. 1968 Aug;66(2):328-32. doi: 10.1016/0002-9394(68)92083-7.
Zotero 插件