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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 9, 2023. (Total: 217811Documents)
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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
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