The pedigree analysis was correct and proved in Mendelian inheritance.
正常家系分析结果符合孟德尔遗传规律。
Methods Clinical observation and pedigree analysis were undertaken in a family with ectopia lentis.
方法对单纯性晶状体异位一家系进行临床研究和系谱分析。
Conclusion Com bined with pedigree analysis, it was summarized that achondroplasia patients in this family might result from this new mutation.
结论结合系谱分析，这一新突变可能是导致该家系患者软骨发育不全的原因。
Pedigree analysis and simple sequence repeats (SSR) were used to analyze the relationship among main released wheat cultivars in Henan Province.
利用系谱分析和SSR标记对河南省小麦主要推广品种间的亲缘关系进行了研究。
Obligate heterozygote --- An individual who may be clinically unaffected but on the basis of pedigree analysis must carry a specific mutant allele.
遗传上已确认为携带特异的突变等位基因，但临床上还未发病的个体。
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。
SSR markers as an effective genotyping technology that can generate enough allelic polymorphism, has become an effective means of breeding pedigree analysis.
SSR标记作为一种有效的基因型鉴定技术，能够产生足够多的等位多态性，已成为育种系谱分析的有效手段。
Method: After pedigree analysis, the prevalence rate of cancer was compared among families with Schizophrenia and with Affective disorder and normal controls.
方法：采用精神分裂症和情感障碍的家系分析法和对照比较法。结果：（1）情感障碍的癌家族发生率最高。
The molecular phylogenetic trees constructed by UPMGA method showed the genetic relationship among 31 restorer lines, which was identical with pedigree analysis.
由UPMGA方法得到的聚类分析结果表明了31个恢复系间的亲缘关系，聚类结果与它们的系谱关系基本吻合。
Microsatellite marker is one of the frequently used molecular markers. It has been used in the genotype identification, pedigree analysis and estimation of genetic distance.
微卫星是近几年来应用较多的一种分子标记，可有效地进行基因鉴定与系谱分析，并可估算群体间的遗传距离。
SSR markers can be expected to complement existing RFLP maps, are useful for genotype identification, gene and QTL analysis, marker assisted selection in breeding and pedigree analysis.
大豆的微卫星标记可扩充现有的RFLP图谱，广泛应用于基因型鉴定，基因和QTL分析，分子标记辅助育种和家系分析等。
The function and menu structure of the computer program package of the population and pedigree analysis of human and medical genetics designed by C language are described briefly in this paper.
本文介绍我们用C语言编制的人类与医学遗传学群体与家系资料分析计算机系统的菜单结构与各子系统的功能。
SSR can be expected to complement existing RFLP, RAPD, AFLP maps, and are useful for genotype identification. gene and QTL analysis, marker assisted selection in breeding and pedigree analysis.
林木的微卫星标记可扩充现有的RFLP、RAPD、AFLP遗传图谱，以及QTL分析，并应用于基因型鉴别，分子标记辅助选择育种。
Pedigree is one of the most general population structure in the genetic linkage analysis between human single genetic inheritance disease locus and genetic marker locus.
在人类单位点致病基因与遗传标记基因的遗传连锁分析中，家系是应用得最普遍的一种群体结构。
The analysis of the pedigree indicated that all the patients inherited their DMD genes from their mothers.
家系分析指出所有病人身上DMD基因都来自于他们的母亲。
Analysis of HLA pedigree in an epidermodysplasia verruciformis family is reported. It was the first report in our country. We have been followed up for 13 years.
报道一个疣状表皮发育不良家族的HLA系谱分析结果，并随访观察13年。
Analysis on the pedigree of several high quality wheat varieties in Shanxi province, and their genetic source of super quality and other main agronomic characters were analysed in this paper.
对山西省几个优质小麦品种进行了系谱追溯，分析了其优质性状及其它主要农艺性状的遗传来源。
Their difference lies in that archeology is a kind of discourse analysis which tries hard to avoid the influence of social system while pedigree stresses the analysis of power.
不同之处在于：其考古学是一种尽力摆脱社会制度影响的话语分析，而其谱系学则着重权力分析。
Methods the parameter linkage analysis of the small pedigree data was used.
方法运用小家系资料连锁分析参数的方法。
The two mutations were confirmed through restriction analysis and pedigree study.
两个突变通过酶切分析和家系调查得到进一步确证。
Both UPGMA cluster and PCA analysis showed clear genetic relationships between the 24 mulberry cultivars. The major clusters were related to known pedigree relationships.
UPGMA法聚类和PCA分析都清楚地显示了24个桑树选育品种的亲缘关系，聚类结果与桑树品种的系谱基本一致。
Presented in this paper are classification of hereditary hearing impairment and methods to perform probability analysis using features of pathogenic genes and information of pedigree.
简要介绍了遗传性耳聋的分类以及利用致病基因特点和家系信息进行概率分析的方法。
Conclusions it suit to the small pedigree data. Multipoint linkage analysis can not only calculate the recombination and map distance, but also localize the disease gene to one side of the marker.
结论适用于小家系资料的多位点连锁分析，不仅能算出致病基因与标记的重组率和遗传距离，而且能把致病基因定位至遗传标记的一侧。
Conclusions it suit to the small pedigree data. Multipoint linkage analysis can not only calculate the recombination and map distance, but also localize the disease gene to one side of the marker.
结论适用于小家系资料的多位点连锁分析，不仅能算出致病基因与标记的重组率和遗传距离，而且能把致病基因定位至遗传标记的一侧。
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