The allele frequency of ALDH2*1 between alcoholic cardiomyopathy group and alcohol dependent group was significantly higher than that in controls and the allele frequency of ALDH2*2 between alcoholic cardiomyopathy group and alcohol dependent group was significantly lower than that in controls.

嗜酒組和酒精性心肌病組ALDH2*1等位基因的頻率高於對(duì)照(P.01)，ALDH2*2等位基因的頻率低於對(duì)照組(P.01)AA片免费看。

The most common allele was allele 5 with a frequency of 70.6%.

最常見的等位基因是5等位基因（DRD4＊5）大伊人久久，頻率為70.6％。

Mapping of microsatellite markers in two wheat crosses segregating for Pm23 and Pm4b, respectively, in combination with the reported mapping of Pm4a, indicated that the three genes were all linked to the marker Xgwm356 with a distance of 3-5 cM. Allelism between Pm4b and Pm23 was then confirmed, when the progenies of a cross between VPM1 (Pm4b) and Line 81-7241, were shown to be all resistant to a B.

利用獲得的8個(gè)標(biāo)記對(duì)Pm4b進(jìn)行遺傳作圖另类性交在线，結(jié)果表明a大乳日韩人妻无码网站，4個(gè)標(biāo)記與Pm4b連鎖(Xgwm356、Xgdm93精品国产一区二区不卡、Xbar76和Xbarc122)欧美一区黄片。3個(gè)抗白粉病基因(Pm4a、Pm4b和Pm23)均與標(biāo)記Xgwm356連鎖欧美三级一级69，遺傳距離為3-5cMWwwav日韩黄色毛片，等位性測(cè)驗(yàn)證明Pm23與Pm4b為等位基因。

Gene mutations were detected in 25 patients and a 18-year-old girl among 16 families. Trinucleotide repeats of CAG were 73～79. The fragments of abnormal alleles were 380～402bp, and all patients were heterozygous. The copy numbers of normal alleles were 18～40, fragments from 202～270bp. SCV reduction was much obvious compared to MCV, MCV and SCV in lower limb ?ere much more slow than that in upper's. BAEP, VEP were also delayed in latency. The anticipation in parental sex bias were much more obvioius than that in matental's. Cerebellar ataxia was most severe, the next were dysarthria and bulging eyes. Amytrophy was seen only in bed ridden patients. Cerebellar atrophy was more severe than brain stem, cord atrophy was n't observed in all MJD.

結(jié)果檢出10個(gè)家系25例病人及1例癥狀前18歲女孩有MJD基因突變国产国爽视频，CAG三核苷酸重復(fù)73～79次人人爱人人操av，異常等位基因片段長(zhǎng)380～402bp，均為雜合子性A片在线播放；正常人CAG三核苷酸重復(fù)18～40次一级黄片免费视频，等位片段長(zhǎng)200～270bp，電生理發(fā)現(xiàn)MJD的SCV減慢比MCV明顯50岁女人一级A片免费，而下肢的MCV色一区、SCV又較上肢明顯，BAEP91精品国精品国产自在久国产、VEP均有不同程度的潛伏期延長(zhǎng)或波的異常日韩,欧美在线不卡片；MJD的父親遺傳早于母親，進(jìn)展也較塊亚洲中文字幕在线第一页，臨床以小腦性共濟(jì)失調(diào)為突出癥狀欧美黑人巨大激情视频，其次為構(gòu)音障礙、突眼等欧美系列一级二级在线观看，肌肉萎縮僅見于晚期病人欧美三级自拍视频；MRI示小腦萎縮較明顯，腦干萎縮并不嚴(yán)重，未見明顯的頸髓萎縮国产丝袜熟女视频一区。

These were controlled by multiple allels or by loci with allels that segregate independently whereby epistasis also may have played a role.

這些是受復(fù)等位基因或含分離等位基因的位點(diǎn)支配的一级毛片精品免费播放，上位性也可能靠它而起了作用。

Genetic polymorphism and effect of MC4R gene(1) The distribution of genotype is significantly different among 6 breeds.

在外來品種中有更多的等位基因G久久综合网天天桃花网，在地方品種中有更多的等位基因A丁香婷婷五月综合。

It was found that the polymorphism existed not only at the allele level but also at the locus level;many alleles of the microsatellite loci and some of the microsatellite loci had been lost during the process of artificial gynogenesis.

該實(shí)驗(yàn)結(jié)果還發(fā)現(xiàn)不僅草魚的微衛(wèi)星位點(diǎn)上存在等位基因的多態(tài)性，而且微衛(wèi)星位點(diǎn)本身也存在多態(tài)性性香港XXXXX免费视频播放；在人工誘導(dǎo)草魚雌核發(fā)育的過程中不僅存在微衛(wèi)星等位基因快速丟失的現(xiàn)象免费真实处破视频在线观看，而且也存在微衛(wèi)星位點(diǎn)丟失的現(xiàn)象。

A new RHAG mutation was found firstly in Chinese population,it is a 582 C＞T homozygosity mutation in RHAG gene.

首次在中國(guó)人群RhD變異型標(biāo)本中發(fā)現(xiàn)一例新的RHAG等位基因一级黄片中文字模，該等位基因是RHAG外顯子第582位C＞T雜合突變5555视频在线观看。

There were totally 22 alleles of these microsatellite loci, and the number of alleles per locus ranged from 2 to 6. The average homozygosity, average polymorphism information content and average heterozygosity was 41.67%, 0.488 and 0.5833, respectively.

對(duì)這6個(gè)位點(diǎn)的擴(kuò)增產(chǎn)物進(jìn)行分析，結(jié)果顯示：6個(gè)位點(diǎn)共檢測(cè)到22個(gè)等位基因免费女人18毛片A级毛片视，每個(gè)位點(diǎn)的等位基因數(shù)從2個(gè)到6個(gè)不等黄片一级片看一下视频；平均基因純合率為41.67%，平均多態(tài)信息含量為0.488嫖娼视频在线观看，平均雜合度為0.5833黄片在线直播观看入口。

The main clime features included ataxia, hypopsia, axanthocyanopsia and retinal pigmental degeneration. Alleles from 7 to 9 repeats were seen in the other 4 healthy members. GAG repeats from 6 to 21 were found in other 126 SCA patients, 71 family members and 60 healthy controls.

該家系內(nèi)表型正常的4位成員SCA7等位基因CAG重復(fù)數(shù)目為7~9，另126例臨床表現(xiàn)為SCA的患者A片在线观看亚洲成AV、71名表型正常的家系成員及60名健康對(duì)照者SCA7等位基因內(nèi)CAG三核苷酸重復(fù)數(shù)為6~21欧美日韩亚洲综合视频。