有可能，科学家依据哪个能够用来进行测试，可以看到样本中线粒体或Y染色体的遗传相似性。
It's possible scientists could have looked at genetic similarities in the mitochondria or even Y chromosome of samples as well, depending on what's available to test.
脆性X综合征，一个X染色体上的基因突变，是遗传性智力障碍最常见的来源，每4000名男孩和每6000名女孩中就有一名儿童患有该症。
Fragile X syndrome, a single genetic mutation on the X chromosome, is the most common source of inherited mental impairment, affecting one in every 4,000 boys and one in every 6,000 girls.
脆性X综合征，一个X染色体上的基因突变，是遗传性智力障碍最常见的来源，每4000名男孩和每6000名女孩中就有一名儿童患有该症。
Fragile X syndrome, a single genetic mutation on the X chromosome, is the most common source of inherited mental impairment, affecting one in every 4, 000 boys and one in every 6, 000 girls.
遗传性嗜中性白血球减少症是一种常染色体隐性遗传疾病，该疾病导致成体中性粒细胞无法从骨髓迁移到血液中。
Trapped Neutrophil Syndrome is an autosomal recessive disease which results in mature neutrophils being unable to migrate from the bone marrow into the blood.
讨论了激光显微外科术应用于染色体工程等遗传学研究的可能性。
The possibility of laser microsurgery in genetics study such as chromosome engineering was discussed.
主要组织相容性复合物（MHC）是由紧密连锁的高度多态的基因位点所组成的染色体上的一个遗传区域，它在脊椎动物机体的免疫系统中发挥着非常重要的作用。
MHC is a chromosomal region consisting of a group of closely linked loci which are highly polymorphic, and plays a central role in the immune system.
肿瘤易感性与异源物代谢酶遗传多态性和染色体畸变等相关。
Tumour susceptibility is associated with genetic polymorphism of xenobiotics metabolism enzyme and chromosomal aberrations et al.
提出了数组链染色体编码方式，以及基于自适应性变异概率和模拟退火惩罚函数法的适应性遗传算法（AGA）。
This paper proposes the array chain chromosome coding and the Adaptive GA (AGA) that combines the self-adaptive mutation probability and simulation anneal punishment function.
大多数论证认为多基因会引致雄性脱发，而其中最为重要的的是雄激素受体基因，该基因位于X性染色体(对于男性来说遗传自母亲)。
Most likely there are multiple genes that contribute towards MPB, the most important of which appears to be the Androgen Receptor gene, located on the X chromosome (inherited from the mother).
目的：获得X染色体短串联重复序列DXS16遗传多态性在河南汉族人群中的分布状况。
Objective To obtain the distribution of genetic polymorphism of X chromosome specific short tandem repeat loci DXS16 in Han groups of Henan province.
脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。
Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.
也可以破坏遗传性卵巢癌病毒染色体(dna)。
Also can damage the hereditary ovarian cancer virus chromosome (DNA).
目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
短串联重复（STR）是Y染色体NRY区的多态性遗传标记的一种，又称微卫星。
Short tandem repeat ( STR) is one of the genetic polymorphic markers within the NRY region in Chromosome Y, which is also called microsatellite.
报道了一个遗传性小眼症家系的调查结果，该家系属于先天性睑裂狭小综合症，为常染色体显性遗传。
An investigation of a genetic Blepharostenosis family was reported. It was proved that the disease was congenital eyelid syndrome and autosomal dominant inheritance.
目的用染色体畸变试验和胞质阻断微核试验来评价职业性接触抗癌药物的护士的遗传毒性危险性。
Objective to evaluate their genotoxic risk in nurses occupationally exposed to antineoplastic drugs with chromosomal aberration test and cytokinesis-block micronucleus (CBMN) test.
在所有的聚合群体中，都定位到同时影响水稻高产、抗旱、耐盐性的遗传重叠位点，比较集中的分布在第1、3和6染色体上。
Genetic overlapping regions affecting HY, together with DT or st detected in all pyramiding populations were mainly distributed in chromosomes 1, 3 and 6.
遗传性无纤维蛋白原血症是一种由于纤维蛋白原基因缺陷所致常染色体隐性遗传病。
Congenital afibrinogenemia is a rare autosomal recessive disorder, characterized by the complete absence or extremely reduced level of fibrinogen.
作为卒中、痴呆和偏头痛的病因，伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)越来越受到人们的重视。
As one of the causes of stroke, dementia and migraine, cerebral autosomal dominant with subcortical infarcts and leukoencephalopathy (CADASIL) has been paid increasing attention.
家族性肥厚型心肌病是一种以常染色体显性遗传为特征的具有遗传异质性的心脏疾病，它是年轻人心源性猝死的首要病因。
Familial hypertrophic cardiomyopathy (FHCM) is a genetically heterogeneous cardiac disease transmitted as an autosomal dominant trait. It is the leading cause of sudden cardiac death (SCD) in youth.
广泛性焦虑校正分离率为0.225，与常染色体隐性遗传的分离率0.25相比较，差异无显著性（P>0.05）；
The segregative rate in generalized anxiety disorder was 0.225, which was not significantly different (P>0.05) from the segregation rate 0.25 in autosome recessive inheritance.
进行性家族性肝内胆汁淤积（PFIC）是一组常染色体隐性遗传肝细胞源性儿童胆汁淤积症。
Progressive familial intrahepatic choleatasia(PFIC)is an autosomal recessive inherited children liver cholestasis characterized by severe jaundice and pruritus.
甘油激酶缺乏症（GKD）是一种少见的X染色体隐性遗传性代谢缺陷病，可分为单纯型和复合型。
Glycerol kinase deficiency (GKD), a rare X-linked recessive disorder, is classified into two types: isolated and complex.
结节性硬化是一种常染色体显性遗传性疾病。过去临床上主要靠病人有癫痫、智力低下和皮脂腺瘤三大体征来诊断。
Tuberous sclerosis (TS) is an exceptional chromosomal inherited disease, This disease was mainly diagnosed by three clinical appearances: epilepsy, intellectual disturbance, and sebaceous adenoma.
结果：①ATD是一种少见的常染色体隐性遗传性骨软骨发育不良疾病。
Result: ATD is an uncommon autosomal recessive hereditary disorder of osteochondrodysplasia.
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.
B物质通过延长凝血时间，可以破坏遗传性乳腺癌病毒染色体（DNA）；
Material B by extending clotting time that can damage the hereditary breast cancer virus chromosomes (DNA);
丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重亚型。
Harlequin ichthyosis ( HI ) is a severe subtype of autosomal recessive congenital ichthyoses ( ARCI ) .
丑角样鱼鳞病是常染色体隐性遗传性鱼鳞病的一种严重亚型。
Harlequin ichthyosis ( HI ) is a severe subtype of autosomal recessive congenital ichthyoses ( ARCI ) .
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