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    Exome sequencing identifies variants in infants with sacral agenesis von Pitsava, Georgia, Feldkamp, Marcia L., Pankratz, Nathan, Lane, John, Kay, Denise M., Conway, Kristin M., Hobbs, Charlotte, Shaw, Gary M., Reefhuis, Jennita, Jenkins, Mary M., Almli, Lynn M., Moore, Cynthia, Werler, Martha, Browne, Marilyn L., Cunniff, Chris, Olshan, Andrew F., Pangilinan, Faith, Brody, Lawrence C., Sicko, Robert J., Finnell, Richard H., Bamshad, Michael J., McGoldrick, Daniel, Nickerson, Deborah A., Mullikin, James C., Romitti, Paul A., Mills, James L., Brody, Lawrence C., Browne, Marilyn L., Feldkamp, Marcia L., Hobbs, Charlotte, Jenkins, Mary M., Olshan, Andrew F., Reefhuis, Jennita, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Almli, Lynn M., Browne, Marilyn L., Conway, Kristin M., Feldkamp, Marcia L., Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., Moore, Cynthia, Olshan, Andrew F., Reefhuis, Jennita, Keegan, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Bamshad, Michael J., Brody, Lawrence C., Kay, Denise M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Pangilinan, Faith, Sicko, Robert J., Lane, John, Pankratz, Nathan, Bamshad, Michael J., Brody, Lawrence C., Feldkamp, Marcia L., Kay, Denise M., Lane, John, McGoldrick, Daniel, Mills, James L., Nickerson, Deborah A., Pankratz, Nathan, Pitsava, Georgia, Romitti, Paul A., Sicko, Robert J., Pitsava, Georgia, Feldkamp, Marcia L., Kay, Denise M., Lane, John, Mills, James L., Pankratz, Nathan, Pangilinan, Faith, Romitti, Paul A., Almli, Lynn M., Bamshad, Michael J., Brody, Lawrence C., Conway, Kristin M., Cunniff, Chris, Finnell, Richard H., Hobbs, Charlotte, Jenkins, Mary M., McGoldrick, Daniel, Mullikin, James C., Nickerson, Deborah A., Olshan, Andrew F., Reefhuis, Jennita, Keegan, Browne, Marilyn L., Canfield, Shaw, Gary M., Sicko, Robert J., Mills, James L., Romitti, Paul A.

    Veröffentlicht in Birth defects research

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