[1] |
.
Clinical significance of Whole exome sequencing in mechanism research and treament in lung cancer
[J]. Basic & Clinical Medicine, 2019, 39(2): 272-276.
|
[2] |
.
Effect of BRAFV600E mutation on expression of VEGF and MMP-9 in papillary thyroid carcinoma
[J]. , 2019, 39(11): 1578-1582.
|
[3] |
.
Analysis of clinical and gene mutation characteristics in four patients with short chain acyl-CoA dehydrogenase deficiency
[J]. , 2019, 39(11): 1574-1577.
|
[4] |
.
Rare mutation of angiopoietin-like protein 8 gene and severe hypertriglyceridemia
[J]. Basic & Clinical Medicine, 2018, 38(5): 622-625.
|
[5] |
Yu-xiu LI, Yong-sheng CHANG.
Detection of novel mutations related to maturity-onset diabetes of the young
[J]. Basic & Clinical Medicine, 2018, 38(4): 470-474.
|
[6] |
.
Quantitative detection of the KRAS gene mutation in circulating tumor DNA for colorectal cancer
[J]. Basic & Clinical Medicine, 2018, 38(2): 180-184.
|
[7] |
.
Mutations of P16INK4a/CDK4/CCND1 genes in 134 Chinese melanoma patients and their clinical significance
[J]. Basic & Clinical Medicine, 2018, 38(2): 153-157.
|
[8] |
.
Clinical features and genetic detection of a family with hereditary late-onset deafness
[J]. Basic & Clinical Medicine, 2018, 38(12): 1680-1685.
|
[9] |
.
Analysis of clinical features and GNAS mutations in patient with pseudohypoparathyroidism
[J]. Basic & Clinical Medicine, 2018, 38(1): 95-97.
|
[10] |
.
Effect of p53 with R213 mutantion on the expression of p21 in colorectal cancer cells HCT116
[J]. Basic & Clinical Medicine, 2017, 37(5): 663-667.
|
[11] |
.
Relationship between MYH7 gene mutation and the ACE /DD genotype and LVH in essential hypertension
[J]. Basic & Clinical Medicine, 2013, 33(4): 439-443.
|
[12] |
.
A clinical and genetic study of a rare adrenoleukodystrophy kindred
[J]. Basic & Clinical Medicine, 2013, 33(10): 1223-1228.
|
[13] |
.
A Chinese girl with Primary hypertrophic osteoarthropathy (PHO) caused by homozygous novel deletion mutation in HPGD and literature review
[J]. Basic & Clinical Medicine, 2012, 32(6): 656-659.
|
[14] |
QIU Zheng-qing WANG Wei WEI Min QIU Jia-jing ZHANG Han-bing WU Xiao-yan.
Mutation analysis of AGL gene in 7 Chinese patients with glycogen storage disease type III
[J]. Basic & Clinical Medicine, 2011, 31(5): 471-474.
|
[15] |
SUN Xiao-fang CHEN Shi Lin LU, QIU Zheng-qing Xin-hua XIAO,.
Clinical and molecular genetic analysis for a patient with glycogen storage disease Ⅰb
[J]. Basic & Clinical Medicine, 2011, 31(5): 529-533.
|