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MeSH:(Monosomy/genetics*)

1.Cytogenetic study of autosomal monosomies among myelodysplastic syndrome patients.

Lu-Xi SONG ; Qi HE ; Yao ZHANG ; Ling-Yun WU ; Li-Yu ZHOU ; Zheng ZHANG ; Xi ZHANG ; Lian-Ping YANG ; Chun-Kang CHANG

Journal of Experimental Hematology 2012;20(6):1410-1413

2.Genetic analysis of a case with a supernumerary marker derived from chromosome 9.

Qianmei ZHUANG ; Meizhen YAN ; Yuying JIANG ; Xinying CHEN ; Na ZHANG ; Chunling LYU ; Jialing WU ; Yuanbai WANG

Chinese Journal of Medical Genetics 2022;39(12):1410-1414

3.Clinical and genetics characteristics of patients with monosomal karyotype acute myeloid leukemia patients.

Feng CHENG ; Xiaolin MA ; Jinlan PAN ; Yafang WU ; Jun ZHANG ; Yongquan XUE ; Qinrong WANG ; Hong YAO ; Lijun WEN ; Yunfeng SHEN ; Suning CHEN

Chinese Journal of Medical Genetics 2014;31(4):508-510

4.Preimplantation genetic diagnosis for Down syndrome pregnancy.

Yu ZHANG ; Chen-ming XU ; Yi-min ZHU ; Min-yue DONG ; Yu-li QIAN ; Fan JIN ; He-feng HUANG

Journal of Zhejiang University. Science. B 2007;8(7):515-521

6.Detection of chromosome 8 anomalies in ovarian carcinoma by fluorescence in situ hybridization.

Yue-lan DONG ; Chun-hua LI ; Li-xin CHEN ; Huai-ying FENG ; Bao-sheng ZHU

Chinese Journal of Medical Genetics 2003;20(1):59-60

7.Genetic analysis of a case with Pierre-Robin sequence due to partial 1q trisomy and partial 4q monosomy.

Qiuyan ZHANG ; Shanshan GAO ; Li WANG ; Panlai SHI ; Xiangdong KONG

Chinese Journal of Medical Genetics 2021;38(4):369-372

8.Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy.

Fengjin QIN ; Xiaoyan LU ; Yapei FENG ; Peihong TANG ; Gang NIU ; Fan LI ; Jianhai ZHANG

Chinese Journal of Medical Genetics 2016;33(2):231-234

9.Monosomal karyotype among adult acute myeloid leukemia: clinical characteristic and prognostic analysis.

Ru FENG ; Hui LIU ; Naibai CHANG ; Yun FAN ; Jiangtao LI ; Yeping ZHANG ; Wei CHEN ; Haifei WANG ; Yuan TIAN ; Lei PEI ; Shangyong NING ; Baoli XING ; Xiaodong XU

Chinese Journal of Hematology 2014;35(5):393-396

10.Clinical characterization and genetic analysis of a newborn with chromosome 8q21.11 deletion syndrome.

Suli LI ; Weiqing WU ; Jiansheng XIE ; Haifei LI

Chinese Journal of Medical Genetics 2021;38(2):145-149

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