日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Mutation Analysis of Exon 1 in the Hemoglobin Subunit Beta (HBB) Gene in Beta-Thalassemia

β-地中海贫血症中血红蛋白亚基β (HBB) 基因外显子1的突变分析

Kumar, K Sharath; Patil, Mallanagouda M; Bulagouda, Rudragouda; Kadakol, Gurushantappa S

Analysis of Single Nucleotide Polymorphisms of Liver X Receptor Alpha (LXR-α) Gene in Diabetic Kidney Disease

糖尿病肾病中肝X受体α(LXR-α)基因单核苷酸多态性分析

Sinnur, Deepa; Bulagouda, R S; Patil, Sandeep; Patil, Santosh

Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson's Disease in the North Karnataka Population

NOS1基因第29外显子的变异与北卡纳塔克邦人群的帕金森病无关

Bulagouda, Rudragouda; Hegde, Smita; Hegde, Rajat; Hiremath, Ashwini; Wali, G M; Kadakol, Gurushantappa S

Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial Study

非综合征性听力障碍患者连接蛋白26 (GJB2) 基因遗传变异分析:家族研究

Hegde, Smita; Hegde, Rajat; Kulkarni, Suyamindra S; Das, Kusal K; Gai, Pramod B; Bulagouda, Rudragouda S

Clinical profile of hemophilia B patients from Karnataka

卡纳塔克邦B型血友病患者的临床特征

Kulkarni, Sujayendra; Hegde, Rajat; Hegde, Smita; Kulkarni, Suyamindra S; Hanagvadi, Suresh; Das, Kusal K; Kolagi, Sanjeev; Gai, Pramod B; Bulagouda, Rudragouda S

Mutation analysis and characterisation of F9 gene in haemophilia- B population of India

印度B型血友病人群F9基因突变分析与特征分析

Kulkarni, Sujayendra; Hegde, Rajat; Hegde, Smita; Kulkarni, Suyamindra S; Hanagvadi, Suresh; Das, Kusal K; Kolagi, Sanjeev; Gai, Pramod B; Bulagouda, Rudragouda