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MeSH:(Chromosomes, Human, Pair 2/genetics)

1.Loss of heterozygosity on chromosome loci 2, 3, 5, 11, 17, and 18 in aberrant crypt foci of human colon.

Ping YUAN ; Menghong SUN ; Jinsheng ZHANG ; Taiming ZHANG ; Xiongzeng ZHU ; Daren SHI

Chinese Journal of Pathology 2002;31(6):485-490

2.MICM characteristics and typing diagnosis in acute myelogenous leukemia patients (AML-M2) with complex karyotype t (2;21;8)(p12;q22;q22).

Yu MA ; Hai-Xia TONG ; Xin DENG ; Yi ZHAO ; Zhuo-Gang LIU ; Ji-Hong ZHANG

Journal of Experimental Hematology 2009;17(1):12-16

3.Advances in molecular genetics research of IgA nephropathy.

Xiejia LI ; Li XIAO ; Lin SUN ; Fuyou LIU

Journal of Central South University(Medical Sciences) 2011;36(11):1120-1124

4.Identification of EBV chromosomal integration sites in Raji cells by fluorescence in situ hybridization.

Jianming GAO ; Xiaoling LI ; Guiyuan LI

Journal of Central South University(Medical Sciences) 2009;34(1):13-19

5.Influence of uniparental disomy on the conclusion of paternity testing.

Bing KANG ; Dong WU ; Xin WANG ; Hongdan WANG ; Miao HE ; Shixiu LIAO

Chinese Journal of Medical Genetics 2019;36(9):938-942

6.Chromosome microdeletions detected in mental retardation.

Rong LI ; Zheng-yan ZHAO ; Shashidhar PAI

Chinese Journal of Medical Genetics 2004;21(4):379-381

7.Genetic polymorphism of 15 STR on chromosome 2 and 11 in Shaanxi Han people in China.

Xiao-Wei SHI ; Feng-Ling REN ; Dong GENG

Journal of Central South University(Medical Sciences) 2008;33(7):587-591

8.A second protein marker of caveolae: caveolin-2.

Liu-luan ZHU ; Ying CUI ; Yong-sheng CHANG ; Fu-de FANG

Chinese Medical Sciences Journal 2010;25(2):119-124

9.Fluorescence in situ hybridization studies on a myeloid leukemia patient with ins(8;21)(q22;q22.1q22.3).

Ya-fang WU ; Yong-quan XUE ; Shu-xiao BAI ; Jun ZHANG ; Li YAO ; Yong WANG ; Hui-ying QIU ; Juan SHEN ; Jin-lan PAN ; Qin-fen MA

Chinese Journal of Medical Genetics 2009;26(2):203-206

10.A case report of myelodysplastic/myeloproliferative disease unclassifiable with karyotype aberration of trisomy 8 and JAK2 mutation.

Kun LIU ; Chang-Xin YING ; Xue-Dong CHEN ; Xue-Yun ZHOU ; Kun-Yuan GUO

Journal of Experimental Hematology 2012;20(5):1139-1143

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