分家的结果就是新家系的诞生。
我们家系的实际创始人是我祖父的哥哥。
不同种源、不同家系的酶谱基本无差异。
There is no significant difference about zymogram of samples from different provenance and families.
从此以后， 倭马亚家系的繁荣就衰落了。
From this point onward the glory of the omayyad line decays.
研究结论支持它为该家系的致病遗传基因。
The study data supports that it is the disease gene of the Chinese big family.
结果共调查108个癫家系的2919个家庭成员。
Results 2919 siblings in the 108 families with epilepsy were studied.
这时，老的家系消亡了，老家系的财产被新家系分割。
At this time, old stirp dies out, its property being divided by the newborn strips.
目的探讨蒙古族家族性脑卒中一大家系的临床特点。
Object: To explore the clinical specialty of stroke in Mongolian family .
G3635A突变位点是3个家系的分子遗传致病基础。
It showed that G3635A mutation was the pathogenic molecular basis for those patients.
上面所说的家系的隐性遗传是由于整段THRB缺失的原因。
The recessive inheritance in the family described above was caused by complete THRB deletion.
在秦岭火地塘进行了10个美国花旗松全同胞家系的引种试验。
The introduction trial, including 10 full-sib families of Pseudotsuga menziesii from America, was carried in Huoditang of Qinling Mountain.
本文报告广西地区发现的一个壮族异常血红蛋白家系的研究结果。
This paper presents the results of a study of abnormal hemoglobin on a family of Chuang ancestry in Guangxi region.
目的研究我国单纯性晶状体异位家系的致病基因，并确定基因突变。
Objective to identify the mutation gene of a Chinese family with ectopia lentis.
结论该家系的致病基因并不为以上9个基因，值得进行全基因组扫描。
Conclusion These 9 genes are not the susceptibility genes of PD in this family.
目的研究一个遗传性蛋白S（PS）缺陷家系的遗传表型及基因型特征。
Objective To study the phenotype and genotype of a protein S (PS) deficiency pedigree.
摘要目的研究一先天缺牙家系的遗传学特点并探寻其可能的致病基因。
Abstract : Objective To investigate the genetic characteristics of a family with congenital oligodontia and to find the possible disease-causing genes.
目的鉴定并分析1个新的肾上腺脑白质营养不良家系的基因突变类型和位点。
Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophy (ALD).
总之，本研究所采用的定位方法对于这个家系的致病基因的准确定位是合理的。
All in all, it is responsible to apply this kind of positional cloning strategy for finding the disease gene in this big family.
对患有萎缩性肌强直(MD)的4个家系的20名成员进行了临床及电生理调查研究。
Clinical and electrophysiological investigations were made in 20 members from 4 myotonic dystrophy (MD) families.
结果成功地为一个2型糖尿病家系的10名成员建立了永生细胞株，其中4名为患者。
ResultsWe successfully established 10 immortal lymphoblastoid cell lines in the family, and 4 of them suffered from type 2 diabetes.
方法：通过收集六个无亲缘关系的瘢痕疙瘩中国家系的临床资料，寻找它们发病的共同特点。
Methods To search their corporate characteristics of occurrence by collecting the clinical information from six Chinese keloid families among which there was no relationship.
目的应用分子生物学方法判定经家系分析初步认定为X连锁遗传的高度近视家系的遗传方式。
Objective Using molecular biological method to determine the inherited modal of a family which was considered as X-linked high myopia by pedigree analysis.
目的对3名来自不同家系的肾上腺脑白质营养不良(ALD)携带者所怀胎儿进行产前分子诊断。
Objective To carry out prenatal molecular diagnosis on 3 fetuses from different pedigrees with X-linked adrenoleukodystrophy (ALD).
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：报告及分析高发癌家系的遗传方式，探讨癌家族肿瘤发生与遗传、环境及饮食习惯之间的关系。
Objective: to know the hereditary pattern of a pedigree with multi-cancer history and to explore the relationship between pathogenesis and heredity, environment and dietary pattern in cancer family.
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.
病例核心家系的RR、归因危险度(AR) %也明显较高，进一步说明血缘关系与NIDDM之间有较强的联系。
RR and the attributable risk (ar) % in the case nuclear family were also higher. It means that there was a strong relationship between blood relatives and NIDDM.
经过10 ~15年无性系测定后，常常将属于几个家系的25 ~50个无性系混合起来，大量投入生产使用。
After 10 to 15 years of clonal testing, mixture of 25 to 50 clones, often belonging to several families, have been released for commercial use.
目的明确一个无明显痴呆的舞蹈病家系的临床、影像学特征及IT15、DRPLA、JPH3、TBP基因突变情况。
Objective To study the clinical, neuroimaging features and identify the mutations of IT15, DRPLA, JPH3 and TBP genes in a large Chinese family of chorea.
目的明确一个无明显痴呆的舞蹈病家系的临床、影像学特征及IT15、DRPLA、JPH3、TBP基因突变情况。
Objective To study the clinical, neuroimaging features and identify the mutations of IT15, DRPLA, JPH3 and TBP genes in a large Chinese family of chorea.
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