染色体

In the end, wavelet neural network after being trained is used to approximation of function to performance good

本文提出的遗传算法利用分级染色体对小波神经网络的结构和权值进行编码，遗传算法联合进化规则来构建和训练小波神经网络，同时对网络进行进化。

ABSTRACT］ Objective To observe the efficacy and side effects of combined therapy with alltrans retinoic acid, arsenic trioxide (As2O3) and chemotherapeutics for newly diagnosed acute promyelocytic leukemia.

急性早幼粒细胞白血病是急性髓系白血病中的一种独特类型(M3型)，以特异的染色体易位t(15，17)(q22，q21)为特征，形成PMLRARa融合基因，该融合基因是APL发病的分子基础和分子标志。

A study on the chromosome numbers and karyotypes of two species of Artemisia.

标题 两种蒿属植物的染色体数目和核型研究。

BACKGROUND: Neonatal-onset multi-system inflammatory disease, a rare autosomal dominantly inherited disease, belongs to a growing spectrum of autoinflammatory diseases, is characterized by urticarial rash, arthropathy, and chronic aseptic meningitis, and is associated with mutations in the cold-induced autoinflammatory gene, CIAS1, the gene that encodes the protein, cryopyrin.

背景：新生儿开始发病的多系统炎性病是一种罕见的常染色体显性遗传性疾病，属于自身炎性疾病逐渐庞大的范畴，表现特征为荨麻疹、关节病和慢性无菌性脑膜炎，它合并有冷刺激诱发的自身炎性基因 CIASI 的突变，该基因是编码蛋白质和 cryopyrin 。

Five patients were alive, they appeared progressive muscular atony and atrophy, especially in shoulder and pelvic girdle, with normal serum creatine kinase and troponin T examination; some patients appeared heart enlargement, arrhythmia, and heart failure.

结论该家系符合常染色体显性遗传的特点；根据患者临床及病理特点，诊断为肢带型肌营养不良症伴心肌损害，以肢带型肌营养不良症ⅠB型可能性大；进一步明确其基因分型需行分子遗传学检查。

In the self-bred progenies of autopolyploid,we found that a very few chimaeraexist in the cells of root tips,but most of them had no change in ploidy. We also found13 diploid plants in the experimental plot (ratio is 0.46%) and can be divided into 4categories.

在部分同源多倍体株系的自交结实后代中，随机取样进行根尖染色体检查，结果表明多倍株系体的自交结实后代倍性没有变化，但发现有个别细胞为不同倍性的嵌合体；田间观察到分离出来的极少数正常二倍体，占0.46％，按照形态特征可以分成四个不同的类型。

Methods Chromosome, HE stainings and autoradiography were made for the cornea of human and monkey.

对猴及人角膜做染色体染色、HE染色及放射自显影。

Objective To explore the application value of STRs of X-chromosome and autosome in Duo-cases.

目的 探讨X-STR和常染色体STR在二联体亲权鉴定中的应用价值。

Pedigree analysis reveals that it is consistent with autosome dominant inheritance.

用家系法分析，符合常染色体显性遗传。

A disease caused by the presence of two recessive mutant genes on an autosome.

由于常染色体上出现突变基因而导致的疾病。

They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.

他们没有侵略性，但我大喊，并在他们的方向扔石头让他们过的线索，远离我，以防万一。

In slot 2 in your bag put wrapping paper, quantity does not matter in this case.

在你的书包里槽2把包装纸、数量无关紧要。