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MeSH:(Chromosomes, Human, Pair 16/*genetics)

1.Molecular cytogenetic analysis for a familial complex chromosomal rearrangement.

Wei-ping QIAN ; Yue-qiu TAN ; Wai-mui TJIA ; Dan SONG ; Xin-yuan GUAN ; Guang-xiu LU

Chinese Journal of Medical Genetics 2005;22(3):302-304

2.Genome-wide genetic study of medulloblastoma using allelotype analysis.

Xiao-lu YIN ; Chung-Sean PANG ; Ho-Keung NG

Chinese Journal of Pathology 2004;33(5):413-415

3.Study of trisomy 22 and inversion 16 in acute myeloid leukemia.

Hui-fen ZHOU ; Jian-yong LI ; Jin-lan PAN ; Hai-rong QIU ; Li-juan CHEN ; Jie-ying HU ; Yun-feng SHEN ; Wei XU ; Yong-quan XUE

Chinese Journal of Hematology 2007;28(1):11-14

4.Clinical and experimental studies on five cases of acute myeloid leukemia with translocation t(16;21)(p11;q22).

Yafang WU ; Yongquan XUE ; Jinlan PAN ; Qinfeng MA

Chinese Journal of Medical Genetics 2003;20(2):171-173

5.Detection of inv (16) in acute myelomonocytic leukemia by interphase fluorescence in situ hybridization.

Jianyong LI ; Jinlan PAN ; Yafang WU ; Yu GUO ; Yongquan XUE

Chinese Journal of Hematology 2002;23(1):30-32

6.Clinical manifestations and genetic diagnosis of paroxysmal kinesigenic dyskinesia.

Xiao-Ming ZHU ; Yu-Hong GONG ; Si LU ; Shou-Chao CHENG ; Bao-Zhen YAO

Chinese Journal of Contemporary Pediatrics 2017;19(11):1169-1173

7.Clinical features and genetic analysis of two cases with 16p13.3 microdeletion and 19q13.4 microduplication derived from familial cryptic balanced translocation.

Huihui XU ; Xing JI ; Lin NI ; Yue ZHU ; Yingwei CHEN ; Bing XIAO

Chinese Journal of Medical Genetics 2016;33(4):490-493

8.Study on the detection of inv(16) in acute myelomonocytic leukemia (M4) by flucorescence in situ hybridization method.

Ying CAI ; Jing-Hua WANG ; Jian ZHANG ; Juan-Hua SHI ; Xi JIN

Journal of Experimental Hematology 2004;12(6):748-751

9.Clinical and genetic study of a child with mental retardation and multiple congenital anomalies and a 16p13.11 microdeletion.

Huanhuan WANG ; Bing XIAO ; Hui YE ; Qin HU ; Wenjuan QIU

Chinese Journal of Medical Genetics 2016;33(4):485-489

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