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Balanced reciprocal whole-arm translocation t(1;19) in three generations.

作者信息

Schober A M, Fonatsch C

出版信息

Hum Genet. 1978 Jun 27;42(3):349-52. doi: 10.1007/BF00291319.

DOI:10.1007/BF00291319
PMID:566714
Abstract

Seven carriers of a balanced reciprocal whole-arm translocation of chromosomes 1 and 19 were found in 19 members investigated in three generations of one family. The apparent lack of a carrier of an unbalanced form of the translocation and of a history of miscarriages are discussed.

摘要

相似文献

1
Balanced reciprocal whole-arm translocation t(1;19) in three generations.
Hum Genet. 1978 Jun 27;42(3):349-52. doi: 10.1007/BF00291319.
2
Familial balanced reciprocal translocation t(1;16) (q12;p13) ascertained because of multiple abortions in a carrier.由于携带者多次流产而确定的家族性平衡易位t(1;16)(q12;p13) 。
Hum Hered. 1977;27(5):362-5. doi: 10.1159/000152891.
3
Reciprocal translocation with special reference to reproductive failure.特别是关于生殖失败的相互易位。
Hum Genet. 1980;55(3):303-7. doi: 10.1007/BF00290208.
4
Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report.携带t(2;7)(p11.2;q22)的患者进行胚胎植入前基因诊断后成功妊娠,其精子和胚胎染色体不平衡率较高:一例报告
Prenat Diagn. 2008 Jan;28(1):36-41. doi: 10.1002/pd.1899.
5
Segregation of two independent chromosomal translocations in one family.
Hum Genet. 1984;68(1):93-5. doi: 10.1007/BF00293881.
6
[Union of 2 carriers of a balanced translocation. Familial study of 3 generations].
Ann Genet. 1985;28(3):164-6.
7
Reciprocal balanced translocation: infertility and recurrent spontaneous abortions in a family.相互平衡易位:一个家族中的不孕和复发性自然流产
Andrologia. 2011 Feb;43(1):75-7. doi: 10.1111/j.1439-0272.2009.01017.x. Epub 2010 Dec 19.
8
Successive spontaneous abortions including one with whole-arm translocation between chromosomes 2.连续自然流产,其中一次流产胎儿存在2号染色体间的全臂易位。
Hum Genet. 1978 Jan 19;40(2):221-5. doi: 10.1007/BF00272305.
9
A balanced whole arm reciprocal translocation resulting in three different adverse pregnancy outcomes.一种平衡的全臂相互易位导致三种不同的不良妊娠结局。
J Med Genet. 1993 May;30(5):417-8. doi: 10.1136/jmg.30.5.417.
10
Familial translocation, t(2;5) (p23; g31).家族性易位,t(2;5) (p23; g31)。
Clin Genet. 1975 Aug;8(2):112-6.

引用本文的文献

1
Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.家族性全臂易位(1;19)、(9;13)和(12;21):101例染色体组型交换的综述
J Appl Genet. 2007;48(3):261-8. doi: 10.1007/BF03195221.
2
Balanced reciprocal whole arm translocation t(3;9): analysis by fluorescence in situ hybridisation.平衡相互性全臂易位t(3;9):荧光原位杂交分析
J Med Genet. 1994 Jan;31(1):74-5. doi: 10.1136/jmg.31.1.74.
3
Fluorescence in situ hybridization reveals a break in the alpha-satellite DNA of chromosome 1 in a family with a balanced whole-arm translocation.

本文引用的文献

1
Variation of the DNA content of morphologically normal and abnormal spermatozoa in mice sesceptible to irregular meiotic segregation.
J Reprod Fertil. 1974 Jun;38(2):335-46. doi: 10.1530/jrf.0.0380335.
2
[Genetic analysis of families with reciprocal translocations].
Genetika. 1973 Nov;9(11):159-64.
3
An analysis of the break points of structural rearrangements in man.人类结构重排断点的分析。
J Med Genet. 1974 Mar;11(1):50-64. doi: 10.1136/jmg.11.1.50.
4
荧光原位杂交显示,在一个患有平衡全臂易位的家族中,1号染色体的α卫星DNA出现断裂。
Hum Genet. 1994 Nov;94(5):504-8. doi: 10.1007/BF00211015.
4
Familial transmission of autosomal whole arm translocation.常染色体全臂易位的家族性传递。
J Med Genet. 1988 Nov;25(11):783-4. doi: 10.1136/jmg.25.11.783.
5
The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments.19号染色体长臂的物理图谱:一些新的定位、确认和重新评估。
Hum Genet. 1991 May;87(1):65-72. doi: 10.1007/BF01213095.
6
Frequency of sister chromatid exchanges in a balanced reciprocal whole-arm translocation.平衡相互全臂易位中姐妹染色单体交换的频率。
Hum Genet. 1979 Sep 2;51(1):93-7. doi: 10.1007/BF00278297.
A simple technique for demonstrating centromeric heterochromatin.
一种用于显示着丝粒异染色质的简单技术。
Exp Cell Res. 1972 Nov;75(1):304-6. doi: 10.1016/0014-4827(72)90558-7.
5
Identification of translocation chromosomes by quinacrine fluorescence.用喹吖因荧光法鉴定易位染色体。
Am J Dis Child. 1972 Jun;123(6):561-4. doi: 10.1001/archpedi.1972.02110120085007.
6
New technique for distinguishing between human chromosomes.区分人类染色体的新技术。
Nat New Biol. 1971 Jul 7;232(27):31-2. doi: 10.1038/newbio232031a0.
7
The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results.染色体结构畸变对人类生殖健康的影响。II. 结果
Clin Genet. 1975 Sep;8(3):169-78. doi: 10.1111/j.1399-0004.1975.tb01490.x.
8
Autosomal reciprocal translocations and 13/14 translocations: a population study.常染色体相互易位与13/14易位:一项群体研究。
Clin Genet. 1976 Sep;10(3):161-77. doi: 10.1111/j.1399-0004.1976.tb00029.x.