CTNS molecular genetics profile in a Persian nephropathic cystinosis population

Autor: Ghazi, Farideh, Hosseini, Rozita, Akouchekian, Mansoureh, Teimourian, Shahram, Ataei Kachoei, Zohreh, Otukesh, Hassan, Gahl, William A., Behnam, Babak

Publikováno v: In NEFROLOGIA (English Edition) May-June 2017 37(3):301-310

Analysis of FGFR3 and HRAS genes in patients with bladder cancer.

Autor: Homami A; Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran., Ataei Kachoei Z; Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran., Asgarie M; Department of Medical Pathology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran., Ghazi F; Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Publikováno v: Medical journal of the Islamic Republic of Iran [Med J Islam Repub Iran] 2020 Aug 28; Vol. 34, pp. 108. Date of Electronic Publication: 2020 Aug 28 (Print Publication: 2020).

CTNS molecular genetics profile in a Persian nephropathic cystinosis population.

Autor: Ghazi F; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran., Hosseini R; Department of Pediatrics, Faculty of Medicine, Ali Asghar Children Hospital, Iran University of Medical Sciences (IUMS), Tehran, Iran., Akouchekian M; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran., Teimourian S; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran., Ataei Kachoei Z; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran., Otukesh H; Department of Pediatrics, Faculty of Medicine, Ali Asghar Children Hospital, Iran University of Medical Sciences (IUMS), Tehran, Iran., Gahl WA; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH, Bethesda, MD, USA., Behnam B; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran; Department of Pediatrics, Faculty of Medicine, Ali Asghar Children Hospital, Iran University of Medical Sciences (IUMS), Tehran, Iran; Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH, Bethesda, MD, USA. Electronic address: Babak.Behnam@nih.gov.

Publikováno v: Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia [Nefrologia] 2017 May - Jun; Vol. 37 (3), pp. 301-310. Date of Electronic Publication: 2017 Feb 24.