家系

血红蛋白ConstantSpring纯合子及其家系调查

A Homozygote for Hemoglobin Constant Spring in Association with its family Study

家族性进行性色素过度沉着症一家系B淋巴细胞系建立及意义

Establishment and Its Significance of B-lymphocyte Cell Lines in A Chinese Family with Familial Progressive Hyperpigmentation

当按区和区内半同胞家系对数据作谱系分析时，我们发现分化很厉害。

When the data were analyzed hierarchically by regions and half-sib families in regions , considerable differentiation was found .

西南地区母系遗传性耳聋家系的线粒体DNA分析

Mitochondrial DNA Mutations in Matrilineal Nonsyndromic Deafness Pedigrees of Southwest China

家族性高脂血症家系血浆载脂蛋白B与代谢综合征的相关性研究

Apolipoprotein B is associated with metabolic syndrome in Chinese pedigrees with familial hyperlipidemia

两例疑为X连锁型视网膜色素变性家系的单倍型分析研究

Haplotype analysis of two families with X - linked retinitis pigmentosa

X染色体倒位伴X连锁无汗性外胚叶发育不良一个家系的产前诊断

Prenatal diagnosis of X-linked anhidrotic ectodermal dysplasia with X-chromosome inversion

N）BRCAI突变见于26.7%（4／15）的SLI6Lwe家系，在家族性乳腺癌患者中为17.40（4／23）；

Mutations in family breast cancer patients were 17.4 % ( 4 / 23 ) .

以颅内占位病变为主要症状的AIDS病一例及母子感染家系报道

One AIDS case with intracranial space-occupying lesion and mother to child transmission

花生F（4∶5）家系产量性状配合力分析

Analysis on combining ability of yield traits in peanut

湿地松优良半同胞家系光和CO2响应曲线特征参数的变异规律

The variance rule of character parameters responding to light and CO_2 of slash pine 's half-sib

X性联锁遗传鱼鳞病一家系的STS基因研究

Investigation of STS Gene in a Pedigree with X-Linked Ichthyosis

湖北地区血红蛋白病研究两个快速β链异常血红蛋白&HbNewYork家系

Study on Hemoglobinopathy in Hubei Province : Two Families of Hb New York (β 113 Val → Glu ) of Fast-moving β - chain Abnormal Hemoglobin

两个遗传性凝血因子Ⅻ缺陷症家系FⅫ基因突变分析

Analysis of the factor ⅻ gene mutations in two Chinese pedigrees with congenital clotting factor ⅻ deficiency

基因分析，抽提家系成员的DNA，进行PCR扩增，扩增片段长度多态性的检测采用银染色法。

DNA from the family members was assayed by PCR and the amplified fragment length polymorphism by silver staining method .

甲型血友病产前诊断&应用DNA聚合酶链反应（PCR）进行家系RFLP连锁分析

The Prenatal Diagnosis of Hemophilia A & The Use of PCR and Family RFLP Analysis

方法采用单因素分析、Logistic多元回归等方法对391个血压异常（高血压或低血压）的核心家系资料进行流行病学分析。

Methods 391 core pedigrees with abnormal blood pressure were analyzed by univariate and multivariate logistic regression .

瘢痕疙瘩家系p53基因的突变

P53 gene mutations in keloid pedigrees

对80例不育男性和30例正常生育男性及12例Yqh~+携带者家系作了染色体C带异态性定量研究。

C-band heteromorphism was studied quantitatively in 80 cases of infertile males , 30 cases of normal fertile males and 12 members of Yqh + bearing families .

Leber遗传性视神经病变家系线粒体DNA突变检测

MtDNA mutation detection in Leber hereditary optic neuropathy families

结果结合临床表现，脑磁共振（MRI）表现与家系分析，患者ALD诊断明确；

Results Diagnosis of ALD was determined by the clinical manifestations and brain MRI .

结论：两个家系先证者的FⅦ缺陷症基因型与其临床表型无明显相关性。

Conclusion : the genotypes were not related with the clinical phenotypes in two probands with hereditary coagulation factor VII deficiency .

在干旱胁迫时，杉木的优树家系中，以39号表现出较小的质膜透性和较高的SOD及POD活性。

Under drought stress Chinese fir family 39 showed less electrolytic leakage and higher SOD , POD activities .

本文用显微切割，PCR技术和染色体绘画技术，构建了人类第七号染色体特异性探针池，并完成了一个7号染色体结构异常患者的家系分析。

We constructed a chromosomal specific probe pool from human chromosome No. 7 using the techniques of chromosomal microdissection , PCR and chromo -

遗传性IgM肾病一家系三例报告及文献复习

Hereditary IgM nephropathy : report of three cases in a kindred and review of literatures

儿童系统性红斑狼疮与HLA基因单倍型和基因型的相关性及家系分析

Association of HLA-A , B , and DR haplotypes with genotype in Chinese children with systemic lupus erythematosus

目的：对一个常染色体显性遗传扩张型心肌病（familialdilatedcardiomyopathy，FDCM）家系进行基因定位。

Objective To localize the gene of autosomal dominant familial dilated cardiomyopathy with conduction defect .

目的：检测并分析一中国先天性长QT综合征（congenitallongQTsyndrome，LQTS）家系的基因突变。

Objective : To identify the gene mutation in a Chinese family of congenital long QT syndrome ( LQTS ) .

基因分型技术首次应用于类孟买型家系ABO基因的研究

Genotyping of ABO blood group in a family of para-Bombay type in Chinese firstly

目的探讨血清结合珠蛋白（HP）水平与2型糖尿病家系胰岛素抵抗（IR）的关系。

Objective : We studied the relationship between haptoglobin ( HP ) and insulin resistance ( IR ) in type 2 diabetes pedigrees .