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Missense Variants in GFRA1 and NPNT Are Associated with Congenital Anomalies of the Kidney and Urinary Tract.
Al-Hamed, Mohamed H; Sayer, John A; Alsahan, Nada; Edwards, Noel; Ali, Wafaa; Tulbah, Maha; Imtiaz, Faiqa.
Affiliation
  • Al-Hamed MH; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Sayer JA; College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
  • Alsahan N; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK.
  • Edwards N; Renal Services, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne NE7 7DN, UK.
  • Ali W; Department of Obstetrics and Genecology, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
  • Tulbah M; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK.
  • Imtiaz F; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
Genes (Basel) ; 13(10)2022 Sep 21.
Article in En | MEDLINE | ID: mdl-36292572
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urinary Tract Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Newborn Country/Region as subject: Asia Language: En Journal: Genes (Basel) Year: 2022 Type: Article Affiliation country: Saudi Arabia
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Urinary Tract Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Newborn Country/Region as subject: Asia Language: En Journal: Genes (Basel) Year: 2022 Type: Article Affiliation country: Saudi Arabia