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Mating between two balanced translocation carriers in two unrelated families.

作者信息

Dallapiccola B, Chessa L, Brinchi V, Frontali M, Gandini E

出版信息

Hum Genet. 1983;65(2):165-8. doi: 10.1007/BF00286655.

DOI:10.1007/BF00286655
PMID:6654331
Abstract

Partial trisomy 9p and a 13/14 translocation occurred in the daughter of a t(5;9)(p15;p12) mother and a t(13;14)(p11;q11) father. Two additional offspring displayed a normal karyotype and a translocation trisomy 13 respectively. Two first cousins, selected for chromosome analysis because of a spontaneous abortion, were found to have an identical translocation t(14;21)(p11;q11). Their second pregnancy was monitored by midtrimester amniocentesis and disclosed a balanced fetus. The different zygotic chromosome constitutions and the counselling problems in the marriages between two balanced translocation carriers are discussed.

摘要

相似文献

1
Mating between two balanced translocation carriers in two unrelated families.
Hum Genet. 1983;65(2):165-8. doi: 10.1007/BF00286655.
2
Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).由于母亲的相互易位rcp(9;21)(p11;q11)出现不同的3:1分离,导致兄弟姐妹中出现9号染色体短臂三体和异常易位型唐氏综合征。
Hum Genet. 1978 Jun 27;42(3):251-6. doi: 10.1007/BF00291304.
3
The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31).
Hum Genet. 1980;55(2):199-202. doi: 10.1007/BF00291767.
4
Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.一名畸形男童20号染色体短臂末端至q11三体,其母亲为t(13;20)(p11;q11)易位携带者。
Hum Genet. 1980 Feb;53(2):169-72. doi: 10.1007/BF00273490.
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An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.一种导致两例15号染色体部分三体的遗传性易位t(4;15) (p16;q22) 。
Ann Genet. 1975 Jun;18(2):99-103.
6
Double balanced chromosomal translocation carrier (6;8), (13;14)--a case report.双平衡染色体易位携带者(6;8),(13;14)——病例报告
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8
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Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24).由于母亲的平衡易位46,XX,t(14;16)(q11;q24)导致的三级三体,47,XX,+14q-- 。
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A 6p trisomy detected in a family with a "giant satellite".在一个有“巨大卫星”的家族中检测到6号染色体三体。
Humangenetik. 1975 Oct 20;30(1):63-7. doi: 10.1007/BF00273632.

引用本文的文献

1
Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal loss.一对反复发生胎儿丢失的夫妇中,男方为罗伯逊易位t(13q;14q),女方为相互易位t(7p;13q) 。
J Med Genet. 1984 Dec;21(6):463-4. doi: 10.1136/jmg.21.6.463.

本文引用的文献

1
The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31).
Hum Genet. 1980;55(2):199-202. doi: 10.1007/BF00291767.
2
Genetic risks for familial reciprocal translocations with special emphasis on those leading to 9p, 10p and 12p trisomies.家族性相互易位的遗传风险,特别强调那些导致9号染色体短臂、10号染色体短臂和12号染色体短臂三体的风险。
Ann Hum Genet. 1982 Jan 1;46(1):41-74. doi: 10.1111/j.1469-1809.1982.tb00694.x.
3
[Study of progeny of individuals bearing a t(DqDq) translocation].[对携带t(DqDq)易位的个体后代的研究]
Ann Genet. 1970 Mar;13(1):11-8.
4
[2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].
Ann Genet. 1972 Jun;15(2):85-92.