品种的中着丝粒单染色体，将分离到的单染色体放入0。
Narcissus monosomes with middle centromeres were isolated with glass needles with the help of micromanipulator and then put into 0.
选择已经定位染色体的SSR引物对单染色体进行PCR扩增，根据得到的分子标记进行单染色体的鉴定。
Select the SSR primer whose colorant layer is located to do PCR augmentation to the monosome, and certificate the monosome according to the gained molecular label.
证实了这两个片段来自含有B染色体的单雌系AKM46，而且可能是B染色体上的特异基因片段。
The results suggest that the sequence come from AKM46 and might be the specific genes in B chromosome.
单引物pcr是一种只用一条引物就可以克隆已知序列侧翼未知区域的染色体步移方法。
Single primer PCR was a method of chromosome walking to isolate sequences flanking a known DNA sequence with only one primer.
进行了黄瓜单（双单）倍体染色体加倍试验。
The chromosome doubling of haploid and double haploid in cucumber was studied.
FAP是一种单基因遗传病，是由APC基因的突变或缺失引起的(apc)基因是5号染色体上发现的。
FAP is a monogenetic disease and is caused by the mutation or deletion of the adenomatous polyposis coli (APC) gene which is found on chromosome 5.
偶线期时，以同源染色体活跃的、特定的配对(联会)为特征，形成了单倍数的二价染色体。
Synapsis (pairing) the association of homologous chromosomes during the prophase stage of meiosis that leads to the production of a haploid number of bivalents.
玉米的杂交不亲和性是受单基因控制的，为配子体控制型，该基因位于玉米的第四染色体上。
Cross incompatibility in Zea mays is controlled gametophytically by a single locus. The gametophyte gene is located on chromosome 4 in maize.
在同源重组中一条染色体的单链与另一条染色体的单链连接形成的结构。
Structure formed during homologous recombination connection of single strands of one chromosome to the other chromosome.
目前，使用PGD技术，可以测试出许多种不同的疾病，包括非整倍体，单基因病和染色体易位等。
Currently, we are able to perform PGD for many genetic conditions including single gene disorders and chromosome abnormalities.
目的探讨8号染色体三体（8三体）对急性粒单、单核细胞白血病（M4、M5）细胞生物学及临床特征的影响。
Object:To evaluate the prognostic impact of trisomy 8 on cytobiological and clinical features in acute myelomonocytic and monocytic leukemia (M4, M5).
牛白细胞粘附缺陷病(BLAD)是一种常染色体单基因隐性遗传疾病，病因为白细胞表面整合素cd 18亚单位基因突变所致。
Bovine leukocyte adhesion deficiency (BLAD) is autosomal recessive disease. The pathogeny of BLAD is genic mutation of CD18-integrins on the leukocyte.
目的调查y染色体7个STR位点及单倍型的遗传多态性并分析其群体差别。
Objective To investigate the genetic polymorphism of7Y-STR loci and haplotypes and analyze their population difference.
利手和叠腿很可能均为常染色体单基因遗传，利手右型和叠腿右型分别为显性性状；
The hereditary mode of handedness or folding leg was likely the dominant heredity of single gene of autosome, and the right type of them was the dominant character.
目前，已有超过200种单基因遗传性疾病被认为是由X染色体连锁遗传引起的，这些疾病只影响男性胎儿。
At present, more than 200 diseases which have been identified are X-linked, these diseases only affect male fetuses.
主要研究结果如下：1。研究了小青杨单芽茎段培养和愈伤组织再生技术，为进一步开展离体叶片细胞染色体加倍以及原生质体培养奠定了基础。
Results are as follows: 1. Axillary buds culture and callus differentiation were studied in this paper, which provide experience for in vitro chromosome doubling and protoplast culture techniques.
卷舌和尖舌均为常染色体单基因显性遗传，能卷舌型和能尖舌型分别为显性性状；
The hereditary mode of rolling tongue or pointed tongue was the dominant heredity of single gene of autosome, and the can-rolling type or can-pointed type was the dominant character.
这些数据质疑这样的观点，即认为端粒需要单链DNA突起形成一个功能性的封盖结构，并证明在染色体末端的保护问题上，大自然有着灵活的解决方案。
These data challenge the view that telomeres require ssDNA protrusions for forming a functional capping structure and demonstrate flexibility in solutions to the chromosome end protection problem.
杂交结果显示，本研究所获得的单条染色体是黄鳝3号染色体；
The single chromosome obtained in the study is rice field eel chromosome 3;
单倍型分析显示先证者及女儿具有相同的致病单倍型。结论报道了中国人常染色体显性遗传ed MD患者的表现型及基因型。
Haplotype analysis indicated that the proband and her daughter Shared the same causative haplotype. Conclusion This is the first report of the phenotype and genotype of AD-EDMD in Chinese.
对2个完整的三代家系和51个核心家系的系谱分析，发现瓣状甲的遗传特点与常染色体单基因显性性状一致。
Analyzing the data of 51 nuclear families and 2 families with 3 generations, it was found that petaloid toenail had the same hereditary characters as a dominant single-gene trait.
翻舌为常染色体单基因隐性遗传，阳性为隐性性状。
Twisting tongue is the recessive heredity of single gene of autosome, while the positive type is the recessive character.
翻舌为常染色体单基因隐性遗传，阳性为隐性性状。
Twisting tongue is the recessive heredity of single gene of autosome, while the positive type is the recessive character.
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