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[期刊论文] 作者：Xia Jia-hui,
来源：中华医学杂志英文版 年份：1989
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MICRODISSECTION OF HUMAN HIGH RESOLUTION BANDED CHROMOSOME, POLYMERASE CHAIN REACTION D MICROCLONING
[期刊论文] 作者：Deng Han-xiang,He Xiao xuan,Li Lu-yun,Xia Jia-hui,Norio Niikawa,
来源：中华医学杂志英文版 年份：1991
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[期刊论文] 作者：LIU Yan-hui,WANG Jian,WANG Xiu-zhi,LI Li-fen,DAI He-ping,XIA Jia-hui,
来源：中国人民解放军军医大学学报（英文版） 年份：2007
Increasing cases of 9p syndrome have been reported since the first description in 1970.In the present case, a extra segment of the end of chromosome 9p resultin...
[期刊论文] 作者：Xia Jia-hui,Li Lu-yun,Dai He-ping,Xu Jia,Xu Fa-ming,He Xiao-xuan,
来源：中华医学杂志英文版 年份：1984
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[期刊论文] 作者：Xia Jia-hui,Ruan Qing-guo,He Xiao-xuan,Li Ling-li,Huang Lei,Deng Han-xiang,Li Lu-yun,
来源：中华医学杂志英文版 年份：1994
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[期刊论文] 作者：ZHU Hai-yan,WU Ling-qian,PAN Qian,LIANG De-sheng,LONG Zhi-gao,DAI He-ping,XIA Kun,XIA Jia-hui,
来源：中华医学杂志英文版 年份：2006
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Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chin
[期刊论文] 作者：XIE Li,GONG Qi-hua,XIE Zhi-guo,LIANG Zong-min,HU Zheng-mao,XIA Kun,XIA Jia-hui,YANG Yi-feng,
来源：中华医学杂志（英文版） 年份：2007
Background Familial hypercholesterolemia (FH) is a type of dominant autosomal disease that causes high levels of plasma low-density lipoprotein cholesterol (LDL...
Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chin
[期刊论文] 作者：XIE Li,GONG Qi-hua,XIE Zhi-guo,LIANG Zong-min,HU Zheng-mao,XIA Kun,XIA Jia-hui,YANG Yi-feng,
来源：中华医学杂志英文版 年份：2007
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Targeted expression of vascular endothelial growth factor 165 in the hrDNA locus mediated by hrDNA t
[期刊论文] 作者：Zong-min,LUO Hong,YANG Yi-feng,LIU Xiong-hao,XIE Li,XUE Zhi-gang,HU Dong-xu,LIANG De-sheng,XIA Kun,XIA Jia-hui,
来源：中华医学杂志英文版 年份：2007
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[期刊论文] 作者：Xia Jia-hui,Li Lu-yun,Dai He-ping,Hu Shi-quan,He Xiao-xuan,Xu Fa-ming,Xu Jia,Xiao Guang-hui,Hu Xin-de,
来源：中华医学杂志英文版 年份：1982
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[期刊论文] 作者：Li Lu-yun,Xia Jia-hui,Dai He-ping,He Xiao-xuan,Xu Fa-ming,Xu Jia,Xiao Guang-hui,He Hong-en,Hu Xin-de,,
来源：中华医学杂志英文版 年份：1982
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,Intracellular Distribution, Assembly and Effect of Disease-associated Connexin 31 Mutants in HeLa C
[期刊论文] 作者：,Zhi-Ping TAN,Qian PAN,De-Sheng LIANG,Zhi-Gao LONG,Ling-Qian WU,Liang-Qun HUANG,He-Ping DAI,Kun XIA,Jia-Hui,
来源：生物化学与生物物理学报（英文版） 年份：2005
Mutations in connexin 31 (Cx31) are associated with erythrokeratodermia variabilis (EKV),hearing impairment and peripheral neuropathy; however, the pathological...
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