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pro vyhledávání: '"Turriff AE"'
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Turriff AE; Prenatal Genomics & Therapy Section, Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD, USA., Bianchi DW; Prenatal Genomics & Therapy Section, Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD, USA. diana.bianchi@nih.gov.; Office of the Director, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD, USA. diana.bianchi@nih.gov.
Publikováno v:
Nature reviews. Cancer [Nat Rev Cancer] 2024 Oct; Vol. 24 (10), pp. 649-650.
Autor:
Faridi R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health (NIH), Bethesda, Maryland, USA., Yousaf R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health (NIH), Bethesda, Maryland, USA., Gu S; Auditory Development and Restoration Program, NIDCD, NIH, Bethesda, Maryland, USA., Inagaki S; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health (NIH), Bethesda, Maryland, USA., Turriff AE; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., Pelstring K; Division of Medical Genetics, Dayton Children's Hospital, Dayton, Ohio, USA., Guan B; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., Naik A; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., Griffith AJ; Otolaryngology Branch, NIDCD, NIH, Bethesda, Maryland, USA., Adadey SM; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.; Division of Human Genetics, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa., Aboagye ET; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.; Division of Human Genetics, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa., Awandare GA; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana., Morell RJ; Genomics and Computational Biology Core, NIDCD, NIH, Bethesda, Maryland, USA., Tsilou E; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., Noyes AG; GeneDx, Inc., Gaithersburg, Maryland, USA., Sulmonte LAG; GeneDx, Inc., Gaithersburg, Maryland, USA., Wonkam A; Division of Human Genetics, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.; McKusick-Nathans Institute and Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Schrauwen I; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Center, New York, New York, USA., Leal SM; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Center, New York, New York, USA.; Taub Institute for Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, New York, USA., Azaiez H; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA., Brewer CC; Otolaryngology Branch, NIDCD, NIH, Bethesda, Maryland, USA., Riazuddin S; Allama Iqbal Medical Research Centre, Jinnah Hospital Complex, Lahore, Pakistan., Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., Hoa M; Auditory Development and Restoration Program, NIDCD, NIH, Bethesda, Maryland, USA., Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, Maryland, USA., de Dios JK; Division of Medical Genetics, Dayton Children's Hospital, Dayton, Ohio, USA., Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Publikováno v:
Clinical genetics [Clin Genet] 2023 Jun; Vol. 103 (6), pp. 699-703. Date of Electronic Publication: 2023 Mar 13.
Autor:
Turriff AE; Prenatal Genomics & Therapy Section, Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD., Annunziata CM; Women's Malignancies Branch, National Cancer Institute, NIH, Bethesda, MD., Bianchi DW; Prenatal Genomics & Therapy Section, Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health (NIH), Bethesda, MD.; Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD.
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2022 Aug 01; Vol. 40 (22), pp. 2398-2401. Date of Electronic Publication: 2022 Jun 15.
Autor:
Nolen RM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA., Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA., Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., Turriff AE; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA., Brewer CC; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., Zalewski CK; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., King KA; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., Wafa TT; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., Griffith AJ; Otolaryngology Branch, National Institute of Deafness and Other Communication Disorders, National Institutes of Health , Bethesda, MD, USA., Brooks BP; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA., Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health , Bethesda, MD, USA.
Publikováno v:
Ophthalmic genetics [Ophthalmic Genet] 2020 Oct; Vol. 41 (5), pp. 401-412. Date of Electronic Publication: 2020 May 06.
Autor:
Prasov L; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.; Department of Ophthalmology and Visual Sciences, W.K. Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan.; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan., Ullah E; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland., Turriff AE; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland., Warner BM; National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland., Conley J; Section of Pediatric Ophthalmology, Helen DeVos Children's Hospital, Grand Rapids, Michigan., Mark PR; Spectrum Health Division of Medical Genetics, Grand Rapids, Michigan., Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland., Huryn LA; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Mar; Vol. 182 (3), pp. 493-497. Date of Electronic Publication: 2020 Feb 05.
Autor:
Turriff AE; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Cukras CA; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Brooks BP; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Huryn LA; National Eye Institute, National Institutes of Health, Bethesda, Maryland.
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2020 Feb; Vol. 24 (1), pp. 58-59. Date of Electronic Publication: 2020 Jan 11.
Autor:
Turriff AE; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Cukras CA; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Brooks BP; National Eye Institute, National Institutes of Health, Bethesda, Maryland., Huryn LA; National Eye Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: laryssa.huryn@nih.gov.
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2019 Jun; Vol. 23 (3), pp. 163-165.e1. Date of Electronic Publication: 2019 Feb 12.
Autor:
Zein WM; National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Falsini B; National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Tsilou ET; National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Turriff AE; National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Schultz JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Brewer CC; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Zalewski CK; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., King KA; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Muskett JA; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Rehman AU; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Morell RJ; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Griffith AJ; Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States., Sieving PA; National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States.
Publikováno v:
Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2014 Nov 25; Vol. 56 (1), pp. 107-14. Date of Electronic Publication: 2014 Nov 25.