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MeSH:(Codon, Nonsense*)

3.Genome-wide Association Studies for Osteoporosis: A 2013 Update.

Yong Jun LIU ; Lei ZHANG ; Christopher J PAPASIAN ; Hong Wen DENG

Journal of Bone Metabolism 2014;21(2):99-116

5.A Novel MUT Gene Mutation Detected in a Female Infant with Methylmalonic Acidemia.

Woo Sun SONG ; Byung Jin SONG ; Hyung Doo PARK ; Won Duck KIM

Neonatal Medicine 2015;22(1):51-54

6.Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency.

Kai Qi JIA ; Zheng Xian SU ; Hui Lin CHEN ; Xiao Yong ZHENG ; Man Lin ZENG ; Ke ZHANG ; Long Ying YE ; Li hong YANG ; Yan Hui JIN ; Ming Shan WANG

Chinese Journal of Hematology 2023;44(11):930-935

7.Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis.

Lihong BAI ; Liping ZHENG ; Binyuan LI ; Hui HUANG ; Xiaoliu SHI ; Yan YI

Journal of Central South University(Medical Sciences) 2023;48(4):565-574

8.Advances in the roles and mechanisms of nonsense-mediated mRNA decay in embryonic development.

Li-Na XUAN ; Xi-Ya SHEN ; Peng WANG ; Lei-Lei DU ; Fan ZHANG ; Xing-Xing XU ; Zhi-Hui HUANG

Acta Physiologica Sinica 2019;71(2):327-335

9.A Novel-Thalassemic Mutation, Codons 89/90-TG, Found in Two Korean Families.

Young Joon LEE ; Sung Sup PARK ; Jiyeon KIM ; Se Ick JOO ; Seonyang PARK ; Jong Weon CHOI ; Soon Ki KIM ; Kyou Sup HAN ; Jin Q KIM ; Eui Chong KIM ; Myoung Hee PARK ; Han Ik CHO

Korean Journal of Clinical Pathology 2001;21(2):160-163

10.Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report.

Eun Jin CHO ; Yong Chul KIM ; Jin Ho HWANG ; Hajung LEE ; Sung Sup PARK ; So Yeon KIM ; Suhnggwon KIM ; Ho Jun CHIN

Kidney Research and Clinical Practice 2012;31(1):72-75

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