Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Phillips, J A 3rd"'
Autor:
Lawson, W. E., Grant, S. W., Ambrosini, V., Womble, K. E., Dawson, E. P., Lane, K. B., Markin, C., Renzoni, E., Lympany, P., Thomas, A. Q., Roldan, J., Scott, T. A., Blackwell, T. S., Phillips III, J. A., Loyd, J. E., du Bois, R. M., Phillips, J A 3rd
Publikováno v:
Thorax; Nov2004, Vol. 59 Issue 11, p977-980, 4p
Publikováno v:
Southern Medical Journal; Aug1990, Vol. 83 Issue 8, p868-875, 8p
Publikováno v:
Southern Medical Journal; Apr1991, Vol. 84 Issue 4, p498-499, 2p
Autor:
Marney, Annis, Lane, Kirk B., Phillips III, John A., Riley, David J., Loyd, James E., Marney, A, Lane, K B, Phillips, J A 3rd, Riley, D J, Loyd, J E
Publikováno v:
CHEST; Jul2001 Supplement, Vol. 120, p56S-56S, 1p
Autor:
McLean, R H, Niblack, G, Julian, B, Wang, T, Wyatt, R, Phillips, J A, 3rd, Collins, T S, Winkelstein, J, Valle, D
Publikováno v:
In Journal of Biological Chemistry 4 November 1994 269(44):27727-27731
Autor:
de Souza DA; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil. denise_andreass@yahoo.com.br.; Functional Genomics Laboratory, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Paraná, Brazil. denise_andreass@yahoo.com.br.; 61H Travessa Chile, São José dos Pinhais, Paraná, 83035-200, Brazil. denise_andreass@yahoo.com.br., Faucz FR; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil.; Section on Endocrinology and Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD, 20892, USA., de Alexandre RB; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil., Santana MA; Octávio Mangabeira Hospital, Reference Center of Cystic Fibrosis, Salvador, Bahia, Brazil., de Souza EL; Pediatric Division, Federal University of Bahia, Salvador, Bahia, Brazil., Reis FJ; Pneumology Division, Department of Pediatrics, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil., Pereira-Ferrari L; Department of Biomedicine, UniBrasil, Curitiba, Paraná, Brazil., Sotomaior VS; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil., Culpi L; Department of Biomedicine, UniBrasil, Curitiba, Paraná, Brazil., Phillips JA 3rd; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA., Raskin S; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil.
Publikováno v:
Genetica [Genetica] 2017 Feb; Vol. 145 (1), pp. 19-25. Date of Electronic Publication: 2017 Feb 03.
Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies.
Autor:
Reis LM; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA., Tyler RC; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA., Weh E; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA.; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA., Hendee KE; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA.; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA., Schilter KF; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA.; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA., Phillips JA 3rd; Division of Medical Genetics and Genomic Medicine, Vanderbilt University Medical Center, Nashville, TN, USA., Sequeira S; Metabolic Unit, Pediatric Department, Hospital de Dona Estefânia, CHLC, Lisbon, Portugal., Schinzel A; Department of Genetics, Institute of Medical Genetics, Schwerzenbach, Switzerland., Semina EV; Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, WI, USA. esemina@mcw.edu.; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA. esemina@mcw.edu.; Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, WI, USA. esemina@mcw.edu.
Publikováno v:
Clinical genetics [Clin Genet] 2016 Oct; Vol. 90 (4), pp. 378-82. Date of Electronic Publication: 2016 Jul 12.
Autor:
Hannig VL; Department of Pediatrics, Division of Genetics and Genomic Medicine, Vanderbilt School of Medicine, DD 2205 MCN, Nashville, TN, 37232, USA, vickie.hannig@vanderbilt.edu., Cohen MP, Pfotenhauer JP, Williams MD, Morgan TM, Phillips JA 3rd
Publikováno v:
Journal of genetic counseling [J Genet Couns] 2014 Feb; Vol. 23 (1), pp. 64-71. Date of Electronic Publication: 2013 May 31.
Autor:
Dhar SU; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA., del Gaudio D, German JR, Peters SU, Ou Z, Bader PI, Berg JS, Blazo M, Brown CW, Graham BH, Grebe TA, Lalani S, Irons M, Sparagana S, Williams M, Phillips JA 3rd, Beaudet AL, Stankiewicz P, Patel A, Cheung SW, Sahoo T
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2010 Mar; Vol. 152A (3), pp. 573-81.
Autor:
Hamid R; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA. rizwan.hamid@vanderbilt.edu, Hedges LK, Austin E, Phillips JA 3rd, Loyd JE, Cogan JD
Publikováno v:
Clinical genetics [Clin Genet] 2010 Mar; Vol. 77 (3), pp. 280-6. Date of Electronic Publication: 2010 Jan 20.