Chinese Journal of Medical Genetics 2010 Issue 6 Association of genetic and mechanical factors with age of onset of knee osteoarthritis

Association of genetic and mechanical factors with age of onset of knee osteoarthritis
JI Jin-fei;DAI Jin;SHI Dong-quan;JIANG Qing

..............page:672-674

Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population
MENG Dong-mei;HAN Lin;MIAO Zhi-min;LI Chang-gui

..............page:659-663

Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type Ⅱ
CUI Ying-xia;XIA Xin-yi;HUANG Ting-ting;WEI Li;FAN Xiao-bo;YAO Bing;GE Yi-feng;LI Xiao-jun;HUANG Yu-feng

..............page:688-691

Establishment of allele specific primer polymerase chain reaction sequence-based typing and investigation of the polymorphism in exon 3 of HLA-DRB1
ZHU Fa-ming;HE Yan-min;TAO Su-dan;ZHANG Wei;WANG Wei;HE Jun-jun;LV Hang-jun;YAN Li-xing

..............page:639-643

46,xx,t(2,7,12) fu za yi wei yi chuan zi dai 7q bu fen san ti yi li
wu li ; zhao zuo ; zhao ling ; hu yu fen ; yang bo ; jia li zuo ; zhang zhan

..............page:703

Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome
BAI Jin-li;WANG Hong;YANG Yan-ling;SONG Fang

..............page:664-667

Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7 -2A＞G mutation of the gene
LI Qi;HUANG De-liang;ZHU Qing-wen;YUAN Yong-yi;FANG Ru-ping;DAI Pu

..............page:610-615

FGFR2 gene mutation in a Chinese patient with Apert syndrome
DAI Li;LI Na-na;YUAN Yu-mei;LIU Yong;ZHU Jun

..............page:682-684

xin xi dong tai

..............page:630,638,687,696,706,709,713,封3

ran se ti zhen duan yu yi chuan zi xun zhong de duo tai xing wen ti he kun huo
zhang si zhong

..............page:707-709

lao nian yu fei lao nian zu duo fa xing gu sui liu de lin chuang xi bao yi chuan xue he yu hou de bi jiao
zuo ling ; zhou min ; chen tao ; xiao rong ; yang jian he ; jiang nai ke ; zhang yan

..............page:710-711

ran se ti yi chang he xing san jia xi liu li
li lin ; li zuo

..............page:716

jia zu xing pa jin sen bing yi jia xi ba li
qu song bin ; wang de sheng ; gang qiang

..............page:625

A novel deletion mutation in AR gene causes complete androgen insensitivity syndrome in a Chinese family
YUE Lin-lin;WU Ping;XIA Zeng-liang;FAN Chun-yuan;XIA Qing-jie

..............page:631-633

yi li man xing li xi bao bai xue bing gu sui xi bao ran se ti fu za yi wei
lin zuo ; xie lian zhi ; song xiu yu

..............page:721

ran se ti yi chang he xing yi jia xi san li
zhang yuan fang ; wang rui li ; wu zhen lan

..............page:715

9hao ran se ti bi jian dao wei zhe luan bao jiang nei dan jing zi zhu she shu hou rong mao ran se ti xin sheng yi chang yi li
zhang ai ping ; zhang xue hong

..............page:717

yi chuan xing dui cheng xing se su yi chang zheng yi jia xi
duan ling ; duan lei ; xu en jie

..............page:667

46,x,t(x;10)(q22;p15) ran se ti yi chang he xing yi li
wang shao min ; qu lin lin ; wang jun rong ; cai

..............page:658

CTLA-4 gene polymorphism regulates CTLA-4 mRNA stability and protein level in patients with ulcerative colitis
CHEN Zhi-tao;XIA Bing;JIANG Ting;ZHOU Feng;ZOU Kai-fang;GE Liu-qing

..............page:603-609

ran se ti ping heng yi wei ban fan fu zi ran liu chan liu li
jia zuo ; song lan lin ; zeng zuo ; luo zuo ; deng kang ; zhong mei ; yu yan hong

..............page:718

A novel PORCN gene mutation in a patient with focal dermal hypoplasia
LIU Yu-mei;ZHOU Xin;DENG Hui-yan;HE Yu-qing;ZHU Hui-lan;ZHANG Xi-bao

..............page:675-677

Association of genetic polymorphisms of COMT gene with psychiatric disorders
GAO Li-bo;ZHONG Shu-rong;JING Qiang

..............page:650-653

zao qi zi ran liu chan rong mao ran se ti he xing fen xi
guo li ; wu zuo ; fu wen zuo ; wang ting ; pan xiao ying

..............page:720-721

Identification of the new allele D18S1364-10 by sequence analysis
ZHAO Ying;XU Wei-hua;FU Sheng-miao

..............page:704-706

shen jing xian wei liu yi jia xi si li
jiang yi ; lin zhen fang ; xu yan ming

..............page:663

Association of the rs4149601 polymorphism of NEDD4L gene with obesity in Xinjiang Kazakh population
WANG Hong-mei;LI Nan-fang;YAO Xiao-guang;HONG Jing;LUO Wen-li;CHANG Jian-hang

..............page:668-671

Mutation analysis of a Chinese family with spinocerebellar ataxia 7
YU Jia;MA Jian-hua;LEI Jing;LI Hai-tao;ZHANG Xiao-ning

..............page:685-687

Genetic analysis of β-thalassemia mutations in the minority populations of Guizhou province
YU Fang;ZHONG Chun-li;ZHOU Qiang;YANG Yuan;LI Wei;LIU Bing;PAN Shao-jin;TANG Kai-yuan;FANG Rong;JIN Wei-jun

..............page:700-703

Association of the rs9939609 polymorphism of FTO gene with overweight or obesity in Hazakh Children
LI Min;LIU Yang;XU Pei-ru;YE Ming-gang;LIU Yu

..............page:678-681

han jian de ran se ti dao wei er li
liu fang ; shi cai hong

..............page:722

yi chuan xing gu gu tou que xue xing huai si yi jia xi jiu li
xu ying peng ; xie li min ; zhang yue ; zeng wo tan ; li yu bin ; chen xiao jun

..............page:714-715

Mitochondrial ND5 as the causative gene of Leight syndrome
WANG Kang;YAN Chuan-zhu;WANG Guo-xiang;JIAO Jing-song;JIN Miao

..............page:616-619

ran se ti 15p+ he xing yi jia xi de y te yi xing tan zhen jian ce
zhang zuo li ; lu bao ting ; yao juan

..............page:712-713

30 li shou bao ran se ti yi chang he xing de xi bao yi chuan xue yu lin chuang fen xi
zhang xiao zhen ; huo xiao chun ; yu ji ying ; rao zhao ying

..............page:719

Improving the diagnostic method for the SLC25A13 gene 851de14 mutation and analysis of the common mutation frequencies in Quanzhou area
GAO Hong-zhi;LI Qiu-lan;ZHUANG Xiang-long;Kobayashi Keiko;Ushikai Miharu;Saheki Takeyori;HU Wei-peng;ZHOU Chang-wen;LIN Ling

..............page:626-630

Gene mapping of developmental dysplasia of the hip in chromosome 17q21 region
LI Lian-yong;SUN Xue-ke;ZHAO Qun;ZHANG Li-jun;LI Qi-wei;WANG Li-li;GAO Hong

..............page:620-625

jia zu xing zhong zheng ji wu li yi jia xi si li
liu wei liang ; li fang ; jiang hong yu ; ai rong ; sun hui

..............page:615

The mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Henan province
WANG Feng-yu;SHAO Chu-jun;FENG Hui-gen;LI Cong-min

..............page:644-649

Association of DNA methyltransferase 3B gene polymorphism with early-onset schizophrenia
ZHANG Chen;FANG Yi-ru;XIE Bin;DU Ya-song;CHENG Wen-hong;WANG Dong-xiang;YU Shun-ying

..............page:697-699

Copy number variation analysis of a Chinese Han family with autism spectrum disorder
YAN Guo-di;LIANG Ya-yong;WANG Ying;HUANG Wei;ZOU Xiao-bing;Nanbert ZHONG

..............page:654-658

The establishment of the controls for blood group genotyping and the application in the screening of three rare blood groups
WANG Pan;YE Lu-yi;GUO Zhong-hui;ZHU Zi-yan

..............page:634-638

46,xy,t(5;6)(q35;p21.3),14p+ yi li
han rui gang ; zhang jun ; feng kai

..............page:643

Association of the CYP19 gene polymorphism with genetic susceptibility to endometriosis
YANG Xin;CHEN Su-qin;LIU Meng

..............page:692-696