Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Braden Maduro VV"'
Autor:
Ellsworth RE; Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Jamison DC, Touchman JW, Chissoe SL, Braden Maduro VV, Bouffard GG, Dietrich NL, Beckstrom-Sternberg SM, Iyer LM, Weintraub LA, Cotton M, Courtney L, Edwards J, Maupin R, Ozersky P, Rohlfing T, Wohldmann P, Miner T, Kemp K, Kramer J, Korf I, Pepin K, Antonacci-Fulton L, Fulton RS, Minx P, Hillier LW, Wilson RK, Waterston RH, Miller W, Green ED
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2000 Feb 01; Vol. 97 (3), pp. 1172-7.
Publikováno v:
Journal of Molecular Evolution. Sep2007, Vol. 65 Issue 3, p207-214. 8p. 3 Charts, 1 Graph.
Autor:
Miller, Webb1 webb@bx.psu.edu, Makova, Kateryna D.1 kdm16@psu.edu, Nekrutenko, Anton1 anton@bx.psu.edu, Hardison, Ross C.1 rch8@psu.edu
Publikováno v:
Annual Review of Genomics & Human Genetics. 2004, Vol. 5 Issue 1, p15-C-4. 46p. 1 Diagram, 1 Chart, 4 Graphs.
Autor:
Cherqui, Stéphanie1 cherqui@necker.fr, Kalatzis, Vasiliki1 kalatzis@necker.fr, Forestier, Lionel1 lionel.forestier@unilim.fr, Poras, Isabelle2 poras@genoscope.cns.fr, Antignac, Corinne1 antignac@necker.fr
Publikováno v:
BMC Genomics. 2000, Vol. 1, p1-5. 5p. 1 Diagram, 1 Chart.
Publikováno v:
Experimental Biology & Medicine; Mar2018, Vol. 243 Issue 5, p496-503, 8p
Autor:
Quemener, Sylvia, Chen, Jian-Min, Chuzhanova, Nadia, Bénech, Caroline, Casals, Teresa, Macek, Milan, Bienvenu, Thierry, McDevitt, Trudi, Farrell, Philip M., Loumi, Ourida, Messaoud, Taieb, Cuppens, Harry, Cutting, Garry R., Stenson, Peter D., Giteau, Karine, Audrézet, Marie-Pierre, Cooper, David N., Férec, Claude
Publikováno v:
Human Mutation; Apr2010, Vol. 31 Issue 4, p421-428, 8p
Autor:
Summers, Tyrone J., Thomas, James W., Lee-Lin, Shih-Queen, Maduro, Valerie V.B., Idol, Jacquelyn R., Green, Eric D.
Publikováno v:
Mammalian Genome; Jul2001, Vol. 12 Issue 7, p508-512, 05p
Delay and mistakes in the diagnosis of inherited metabolic diseases may have devastating consequences. Reference laboratory data are scattered and clinical descriptions of rare conditions are hard to locate. This book describes 298 disorders, grouped
Autor:
Parker, Philip M., Parker, James N.
Title from e-book title screen (viewed on August 26, 2004)