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MeSH:( Exons/genetics)

1.P53 gene mutation detection by bioluminometry assay.

Guo-hua ZHOU ; Zhuo-liang GU ; Jie-bing ZHANG

Acta Pharmaceutica Sinica 2002;37(1):41-45

2.Study on NPM1 gene mutations in patients with primary myelodysplastic syndromes.

Lin LI ; Yue ZHANG ; Xiao-Tang MA ; Lin YANG ; Ze-Feng XU ; Zhi-Jian XIAO

Chinese Journal of Hematology 2010;31(12):809-812

3.Analysis of mutations in exon 7 of phenylalanine hydroxylase gene among children with phenylketonuria in Ningxia, China.

Xin-Mei MAO ; Jiang HE ; Yuan LIU ; Xiao-Qiang LI ; Wu-Zhong YU ; Zhi-Hui GAO ; Jing CAI

Chinese Journal of Contemporary Pediatrics 2014;16(3):259-262

5.Identification of two novel variants of the PCCB gene in a pedigree affected with propionic acidemia.

Qigang ZHANG ; Guanglai FAN ; Shu ZHANG ; Yuefang LIU ; Wenjie ZHANG ; Qiong PAN

Chinese Journal of Medical Genetics 2021;38(3):251-254

6.Serological and molecular studies of a rare A subgroup.

Bin HAN ; Yuli ZHU ; Yahui QU ; Li LIU ; Zhihui FENG

Chinese Journal of Medical Genetics 2021;38(8):807-808

7.Analysis of an ABO subtype with a novel variation.

Xinming WU ; Fangyuan JI ; Ni HUO ; Linhai ZHANG ; Liping LIU ; Yong YAO

Chinese Journal of Medical Genetics 2022;39(10):1158-1160

8.Different Subtypes Caused by c.721C>T Substitution in the Exon 7 of ABO Gene.

Jian-Yu XIAO ; Chen-Chen FENG ; Tai-Xiang LIU ; Li-Li SHI ; Ruo-Yang ZHANG ; Cheng-Yin HUANG ; Qing CHEN

Journal of Experimental Hematology 2021;29(6):1917-1922

9.Molecular genetic analysis of four cases with weak D variant of Rh blood type.

Yunlei HE ; Gang DENG ; Deyi XU ; Wei LIANG ; Lu YU

Chinese Journal of Medical Genetics 2016;33(6):837-840

10.Genetic analysis for a family affected with hemophilia type A due to a large deletion of F8 gene.

Nan BAI ; Shiyue MEI ; Ning LIU ; Zhenhua ZHAO ; Jingjing MENG ; Xiangdong KONG

Chinese Journal of Medical Genetics 2016;33(6):782-785

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