Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Skvorak, A B"'
Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans
Autor:
Vahava, Oz, Morell, Robert, Lynch, Eric D., Weiss, Sigal, Kagan, Marjory E., Ahituv, Nadav, Morrow, Jan E., Lee, Ming K., Skvorak, Anne B., Morton, Cynthia C., Blumenfeld, Anat, Frydman, Moshe, Friedman, Thomas B., King, Mary-Claire, Avraham, Karen B.
Publikováno v:
Science, 1998 Mar . 279(5358), 1950-1954.
Externí odkaz:
https://www.jstor.org/stable/2895855
Publikováno v:
Human Molecular Genetics; Mar1999, Vol. 8 Issue 3, p439, 14p
Autor:
Karet, Fiona E., Finberg, Karin E., Nelson, Raoul D., Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A., Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J., Pietro, Antonio Di, Hoffbrand, Barry I., Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A., Wu, Doris K., Skvorak, Anne B.
Publikováno v:
Nature Genetics; Jan1999, Vol. 21 Issue 1, p84, 7p
Autor:
Avraham, Karen B., Hasson, Tama, Sobe, Tama, Balsara, Binaifer, Testa, Joseph R., Skvorak, Anne B., Morton, Cynthia C., Copeland, Neal G., Jenkins, Nancy A.
Publikováno v:
Human Molecular Genetics; Aug1997, Vol. 6 Issue 8, p1225-1231, 7p
Autor:
Greinwald, J H, Scott, D A, Marietta, J R, Carmi, R, Manaligod, J, Ramesh, A, Zbar, R I, Kraft, M L, Elbedour, K, Yairi, Y, Musy, M, Skvorak, A B, Van Camp, G, Srisailapathy, C R, Lovett, M, Morton, C C, Sheffield, V C, Smith, R J
Publikováno v:
Genome Research; September 1997, Vol. 7 Issue: 9 p879-886, 8p
Autor:
Robertson, Nahid G., Skvorak, Anne B., Yin, Yi, Weremowicz, Stanislawa, Johnson, Kenneth R., Kovatch, Kristina A., Battey, James F., Bieber, Frederick R., Morton, Cynthia C.
Publikováno v:
Genomics; December 1997, Vol. 46 Issue: 3 p345-354, 10p
Autor:
Skvorak, Anne B., Robertson, Nahid G., Yin, Yi, Weremowicz, Stanislawa, Her, Helen, Bieber, Frederick R., Beisel, Kirk W., Lynch, Eric.D., Beier, David R., Morton, Cynthia C.
Publikováno v:
Genomics; December 1997, Vol. 46 Issue: 2 p191-199, 9p
Autor:
Karet FE; Howard Hughes Medical Institute, Department of Medicine, Yale University School of Medicine, Boyer Center for Molecular Medicine, New Haven, Connecticut 06510, USA., Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP
Publikováno v:
Nature genetics [Nat Genet] 1999 Jan; Vol. 21 (1), pp. 84-90.