Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143-146).

Suppr

超能文献

作者信息

Furlong R A, Lyall J E, Lush M J, Affara N A, Ferguson-Smith M A

机构信息

Department of Pathology, University of Cambridge, UK.

出版信息

Hum Mol Genet. 1992 Sep;1(6):447. doi: 10.1093/hmg/1.6.447.

DOI:10.1093/hmg/1.6.447

PMID:1301917

Abstract

摘要

相似文献

Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143-146).

Hum Mol Genet. 1992 Sep;1(6):447. doi: 10.1093/hmg/1.6.447.

A dinucleotide repeat polymorphism at the D9S127 locus.

Nucleic Acids Res. 1992 Feb 25;20(4):925. doi: 10.1093/nar/20.4.925-a.

Three tetrameric repeat polymorphisms on human chromosome 3: D3S1349; D3S1350; D3S1351.

Hum Mol Genet. 1993 Jun;2(6):819. doi: 10.1093/hmg/2.6.819.

A dinucleotide repeat polymorphism at the D9S749 locus.

Hum Mol Genet. 1994 Sep;3(9):1713. doi: 10.1093/hmg/3.9.1713.

Two dinucleotide repeat polymorphisms at the DXS571 locus.

Hum Mol Genet. 1992 Dec;1(9):776. doi: 10.1093/hmg/1.9.776.

Six dinucleotide microsatellite polymorphisms on human chromosome 3.

Hum Mol Genet. 1993 Jun;2(6):817-8. doi: 10.1093/hmg/2.6.817.

Dinucleotide repeat polymorphism at the human CD59 locus.

Clin Genet. 1995 Mar;47(3):165-6. doi: 10.1111/j.1399-0004.1995.tb03952.x.

Two microsatellite repeat polymorphisms in the EPO gene.

Hum Mol Genet. 1994 Jan;3(1):219. doi: 10.1093/hmg/3.1.219.

An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene.

Hum Mol Genet. 1992 Dec;1(9):781. doi: 10.1093/hmg/1.9.781.

Three new dinucleotide repeat polymorphisms on human chromosome 9: D9S970, D9S971, and D9S972.

Hum Genet. 1995 Aug;96(2):237-8. doi: 10.1007/BF00207389.

引用本文的文献

High prevalence of p16 genetic alterations in head and neck tumours.

Br J Cancer. 1999 Oct;81(4):677-83. doi: 10.1038/sj.bjc.6690747.

Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.

J Med Genet. 1997 Apr;34(4):331-4. doi: 10.1136/jmg.34.4.331.

Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge development.

Hum Genet. 1996 Apr;97(4):506-11. doi: 10.1007/BF02267076.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验