Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Nephrocalcinosis and AGXT[original query] |
---|
Etiological Profile of Nephrocalcinosis in Children from Southern India. Indian pediatrics 2020 3 57 (5): 415-419. Ramya Kagnur, Krishnamurthy Sriram, Sivamurukan Palanisa |
Molecular Diagnosis of Primary Hyperoxaluria Type 1 and Distal Renal Tubular Acidosis in Moroccan Patients With Nephrolithiasis and/or Nephrocalcinosis. Cureus 2022 5 14 (3): e23616. Fatima Abdouss, Mohamed Ahakoud, Moustapha Hida, Karim Ould |
Genetic testing enables a precision medicine approach for nephrolithiasis and nephrocalcinosis in pediatrics: a single-center cohort. Molecular genetics and genomics : MGG 2022 May . Huang Lin, Qi Chang, Zhu Gaohong, Ding Juanjuan, Yuan Li, Sun Jie, He Xuelian, Wang Xiaow |
Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease-associated pathogenic variants. Clinical genetics 2022 10 103 (1): 53-66. Abid Aiysha, Raza Ali, Khan Abdul Rafay, Firasat Sadaf, Shahid Saba, Hashmi Seema, Zafar Mirza Naqi, Sultan Sajid, Khaliq Shagufta, Rizvi Syed Adib-Ul-Has |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
- Content source: