通过喹吖因荧光鉴定的涉及6号、14号和20号染色体的家族性易位。 - Suppr

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Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.

作者信息

Allderdice P W, Miller O J, Miller D A, Breg W R, Gendel E, Zelson C

出版信息

Humangenetik. 1971;13(3):205-9. doi: 10.1007/BF00326943.

DOI:10.1007/BF00326943

PMID:5114675

Abstract

摘要

相似文献

Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.通过喹吖因荧光鉴定的涉及6号、14号和20号染色体的家族性易位。

Humangenetik. 1971;13(3):205-9. doi: 10.1007/BF00326943.

Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.通过亲代染色体研究检测并鉴定出与家族性F-13易位相关的部分F三体。

J Pediatr. 1971 Apr;78(4):664-72. doi: 10.1016/s0022-3476(71)80471-7.

Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.8号染色体短臂三体：与8号和22号染色体之间的易位相关，46，XY，22 - ，t(8p22q)加。

Clin Genet. 1973 Jun;4(6):507-16. doi: 10.1111/j.1399-0004.1973.tb01940.x.

Banding identification of partial trisomy 15 and of 8/21 translocation.15号染色体部分三体及8/21易位的显带鉴定

J Ment Defic Res. 1974 Jun;18(2):139-44. doi: 10.1111/j.1365-2788.1974.tb01230.x.

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.人染色体的喹吖因氮芥荧光：异常易位的特征

Am J Hum Genet. 1972 Mar;24(2):189-213.

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.推定9号染色体短臂三体性，非遗传性易位所致。

Humangenetik. 1971;12(3):175-81. doi: 10.1007/BF00702772.

Identification of partial 12 trisomy by quinacrine fluorescence.用喹吖因荧光法鉴定部分12三体

J Pediatr. 1973 Feb;82(2):269-72. doi: 10.1016/s0022-3476(73)80165-9.

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.在一名智力发育迟缓的女孩中，通过喹吖因荧光诊断出一条9号环状染色体。

Clin Genet. 1973;4(5):434-41. doi: 10.1111/j.1399-0004.1973.tb01173.x.

Brother and sister with trisomy 10p: a new syndrome.患有10号染色体短臂三体综合征的兄妹：一种新综合征。

Humangenetik. 1974;23(3):163-72. doi: 10.1007/BF00285102.

Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.9号染色体短臂三体综合征患儿母亲中可能存在复杂易位t(9;14;13) (q12;pl?;Q31) 。

Humangenetik. 1974;25(2):83-92. doi: 10.1007/BF00283308.

引用本文的文献

Chromosome Translocation t(6; 14) With Different Phenotypes and Segregation Patterns: A Report of Two Cases.具有不同表型和分离模式的染色体易位t(6; 14)：两例报告

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Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11.2q21.3 in a fetus: a case report.胎儿母体9号染色体短臂23区至24.3区及14号染色体长臂11.2区至21.3区部分三体的产前诊断：病例报告

Mol Cytogenet. 2020 Feb 6;13:6. doi: 10.1186/s13039-020-0473-x. eCollection 2020.

Reproductive possibilities for balanced translocation (14) carriers in families with partial trisomy of proximal 14q.近端14q部分三体家庭中平衡易位（14）携带者的生育可能性。

J Med Genet. 1993 Jan;30(1):73-5. doi: 10.1136/jmg.30.1.73.

A severely retarded 18-year-old boy with tertiary partial trisomy 14.一名患有14号染色体三次部分三体综合征的重度智障18岁男孩。

J Med Genet. 1980 Jun;17(3):230-2. doi: 10.1136/jmg.17.3.230.

Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations.6号、7号、8号和12号染色体复杂重排在三代人中的分离情况。

Hum Genet. 1981;58(2):221-5. doi: 10.1007/BF00278717.

A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.一名表现为不育的表型正常男性中涉及三条常染色体的复杂重排。

J Med Genet. 1982 Oct;19(5):375-7. doi: 10.1136/jmg.19.5.375.

The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.“猫眼综合征”：双着丝粒小标记染色体可能源自22号染色体（22号染色体短臂末端至q11的四体性），伴有特征性表型。11例患者报告及临床表现描述。

Hum Genet. 1981;57(2):148-58. doi: 10.1007/BF00282012.

De novo translocation heterozygote with three reciprocal translocations.具有三个相互易位的新生易位杂合子。

J Med Genet. 1983 Oct;20(5):385-8. doi: 10.1136/jmg.20.5.385.

A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.一例母亲和兄弟患有部分14三体综合征（47,XY,(14q-)+）以及9号染色体短臂增加和14号染色体长臂减少的易位（t(9p+;14q-)）的病例。

J Med Genet. 1972 Sep;9(3):367-73. doi: 10.1136/jmg.9.3.367.

本文引用的文献

Presumptive C-15 translocation and familial large Y identified by autoradiography.通过放射自显影鉴定出推定的C-15易位和家族性大Y染色体。

J Med Genet. 1969 Mar;6(1):89-94. doi: 10.1136/jmg.6.1.89.

A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.一例伴有胎儿血红蛋白持续存在的多重染色体重排病例。

Cytogenetics. 1968;7(3):169-82. doi: 10.1159/000129981.

A complex familial translocation involving chromosomes 5, 9 and 13.涉及5号、9号和13号染色体的复杂家族性易位。

Cytogenetics. 1970;9(4):294-306. doi: 10.1159/000130099.

A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome.一种与唐氏综合征相关的罕见易位（47,XY,t(2p-;21q+),21+）。

J Med Genet. 1970 Dec;7(4):389-93. doi: 10.1136/jmg.7.4.389.

Identification of human chromosomes by DNA-binding fluorescent agents.利用DNA结合荧光剂鉴定人类染色体

Chromosoma. 1970;30(2):215-27. doi: 10.1007/BF00282002.

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