WordNet

(chemistry) the existence of different kinds of crystal of the same chemical compound (同)pleomorphism
(biology) the existence of two or more forms of individuals within the same animal species (independent of sex differences)
(genetics) the genetic variation within a population that natural selection can operate on

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Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: Probability of synergistic effects.

Duraturo F, Liccardo R, Cavallo A, Rosa MD, Grosso M, Izzo P.SourceDepartment of Biochemistry and Medical Biotechnology, Federico II University, Naples, Italy.
International journal of cancer. Journal international du cancer.Int J Cancer.2011 Oct 1;129(7):1643-50. doi: 10.1002/ijc.25824. Epub 2011 Apr 25.
Mutations in the MLH1 and MSH2 genes account for a majority of cases of families with Lynch Syndrome. Germ-line mutations in MSH6, PMS2 and MLH3 are responsible for disease in a minority of cases, usually associated with milder and variable phenotypes. No germ-line mutations in MSH3 have so far been
PMID 21128252

Analysis of genetic diversity and phylogenetic relationship of red deer subspecies in XinJiang, China.

Jia B, Li RY, Zhao ZS, Yan GQ, Xi JF, Blair HT, Li DQ, Zhang JX, Zhao XT.SourceAnimal Science and Technology College, Shihezi University, ShiHeZi, XinJiang Animal Science Institute of Vocational Technology School in Agriculture of XinJiang, ChaJi, XinJiang Bureau of Agriculture in Kuerle Regiment Two of XinJiang, Kuerle, XinJiang, China Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Animal science journal = Nihon chikusan Gakkaih?.Anim Sci J.2011 Aug;82(4):517-22. doi: 10.1111/j.1740-0929.2011.00885.x. Epub 2011 Jun 15.
Polymorphisms for seven microsatellite loci in three red deer subspecies (9 populations) found in XinJiang were detected by polymerase chain reaction (PCR), 12% nondenaturation polyacrylamide gel electrophoresis and the Sanguinetti silver staining method. Numbers of alleles, average effective number
PMID 21794008

1) ゲノム不安定性・遺伝子変異に基づく子宮体癌の浸潤能獲得と分子生物学的予後不良因子の検討(シンポジウム1:腫瘍「婦人科癌の浸潤・転移機構の解明と臨床応用」,第65回日本産科婦人科学会・学術講演会講演要旨)

織田克利
日本産科婦人科學會雜誌 65(10), 2388-2401, 2013-10-01
… Background: Genomic instability, such as chromosomal instability (CI) and microsatellite instability (MSI), is known to be associated with cancer progression in various tumors. … Methods: A comprehensive genomic survey was performed in 47 endometrial carcinomas with paired DNA for chromosomal imbalances by SNP (Single Nucleotide Polymorphism) typing array and screened 32 samples for MSI status. … MSI-high with 3 or more alterations among 5 microsatellite markers was identified in11 (35%) patients. …
NAID 110009674401

津川尚子
ビタミン 87(8), 435-439, 2013-08-25
… Specifically, the influence of rs699664 (Arg325Gln) single nucleotide polymorphism (SNP) in exon 8 and rs10654848 microsatellite in intron 6 on activation of clotting factors or bone metabolism have been reported frequently. … In this report, I would like to review about the kinds of GGCX polymorphism, and its effects on vitamin K action. …
NAID 110009635557