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HL-A antigens and heteromorphic fluorescence characters of chromosomes in prenatal paternity investigation.

作者信息

Jonasson J, Lindsten J, Lundborg R, Kissmeyer-Nielsen F, Lamm L U, Petersen G B, Therkelsen A J

出版信息

Nature. 1972 Apr 7;236(5345):312-3. doi: 10.1038/236312a0.

DOI:10.1038/236312a0
PMID:4552164
Abstract
摘要

相似文献

1
HL-A antigens and heteromorphic fluorescence characters of chromosomes in prenatal paternity investigation.产前亲子鉴定中HL-A抗原与染色体的异形荧光特征
Nature. 1972 Apr 7;236(5345):312-3. doi: 10.1038/236312a0.
2
Quinacrine mustard fluorescence of sex chromatin in human amniotic fluid cell cultures.人羊水细胞培养中性染色质的喹吖因芥子荧光
Nature. 1972 Jan 28;235(5335):226-9. doi: 10.1038/235226a0.
3
[Prenatal sexual determination from amniotic epithelial cells using fluorescent microscopy].
Geburtshilfe Frauenheilkd. 1972 Jan;32(1):20-4.
4
[Present status of prenatal sex-diagnosis (author's transl)].产前性别诊断的现状(作者译)
Z Geburtshilfe Perinatol. 1974 Jun;178(3):149-63.
5
Problems in prenatal diagnosis resulting from chromosomal mosaicism.
Clin Genet. 1972;3(2):83-9. doi: 10.1111/j.1399-0004.1972.tb01730.x.
6
[Cytogenetic paternity test in father-daughter incest (case report) (author's transl)].父女乱伦中的细胞遗传学亲子鉴定(病例报告)(作者译)
Dtsch Med Wochenschr. 1977 Jul 8;102(27):900-1000.
7
[Diagnosis of paternity from peripheral blood granulocytes: study of fluorescence with the use of quinacrine].[外周血粒细胞的亲子鉴定诊断:吖啶橙荧光法研究]
Haematologica. 1973;58(3):227-32.
8
Immunological selection of HL-A variants of cultured progeric fibroblasts and their identification by quinacrine fluorescence.培养的早老性成纤维细胞HL-A变体的免疫选择及其吖啶橙荧光鉴定
Exp Cell Res. 1974 Dec;89(2):451-4. doi: 10.1016/0014-4827(74)90822-2.
9
Identification of Y and X chromosomes in amniotic fluid cells.
Nature. 1971 Mar 5;230(5288):53. doi: 10.1038/230053a0.
10
Technical and theoretical considerations in the HLA typing of amniotic fluid cells for prenatal diagnosis and paternity testing.用于产前诊断和亲子鉴定的羊水细胞HLA分型中的技术和理论考量
Prenat Diagn. 1981 Jul;1(3):183-95. doi: 10.1002/pd.1970010304.

引用本文的文献

1
In utero paternity testing utilizing fetal blood obtained by midtrimester fetoscopy.利用孕中期胎儿镜检查获取的胎儿血液进行子宫内亲子鉴定。
Am J Hum Genet. 1980 Jan;32(1):88-91.
2
Pericentric inversions. Problems and significance for clinical genetics.臂间倒位。临床遗传学中的问题及意义。
Hum Genet. 1984;68(1):1-47. doi: 10.1007/BF00293869.
3
Strongly fluorescent chromosome bands in metaphase and interphase.
Humangenetik. 1974 May 17;22(2):127-32. doi: 10.1007/BF00278451.
4
[Polymorphisms in human chromosomes--a new aid for affiliation cases (author's transl)].[人类染色体多态性——亲子鉴定案例的新辅助手段(作者译)]
Z Rechtsmed. 1974 Mar 29;74(1):17-23. doi: 10.1007/BF01869180.
5
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis.
Hum Genet. 1976 Dec 15;34(3):315-8. doi: 10.1007/BF00295297.
6
Pitfalls in the use of chromosome variants for paternity dispute cases.亲子鉴定案件中染色体变异应用的陷阱。
Hum Genet. 1977 Jul 26;37(3):255-60. doi: 10.1007/BF00393606.
7
A photometric method for quantifying the polymorphisms in human acrocentric chromosomes.一种用于定量分析人类近端着丝粒染色体多态性的光度测定法。
Hum Genet. 1977 Feb 11;35(2):185-91. doi: 10.1007/BF00393968.
8
Chromosome studies in man: past achievements and recent advances.人类染色体研究:过去的成就与近期进展
J Clin Pathol. 1976 Jul;29(7):569-82. doi: 10.1136/jcp.29.7.569.
9
LBA technique in the detection of chromosome variants. I. Chromosomes with known sites of Q variants.LBA技术在染色体变异检测中的应用。I. 具有已知Q变异位点的染色体
Hum Genet. 1977 Nov 2;39(1):31-7. doi: 10.1007/BF00273151.
10
The segregation of C-band polymorphisms on chromosomes 1, 9, and 16.1号、9号和16号染色体上C带多态性的分离
Am J Hum Genet. 1976 Jul;28(4):412-6.