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Exome sequencing identifies variants in infants with sacral agenesis.
Pitsava G, Feldkamp ML, Pankratz N, Lane J, Kay DM, Conway KM, Hobbs C, Shaw GM, Reefhuis J, Jenkins MM, Almli LM, Moore C, Werler M, Browne ML, Cunniff C, Olshan AF, Pangilinan F, Brody LC, Sicko RJ, Finnell RH, Bamshad MJ, McGoldrick D, Nickerson DA, Mullikin JC, Romitti PA, Mills JL; UW Center for Mendelian Genomics, NISC Comparative Sequencing Program and the National Birth Defects Prevention Study. Pitsava G, et al. Among authors: feldkamp ml. Birth Defects Res. 2022 Apr;114(7):215-227. doi: 10.1002/bdr2.1987. Epub 2022 Mar 10. Birth Defects Res. 2022. PMID: 35274497 Free PMC article.
Control selection and participation in an ongoing, population-based, case-control study of birth defects: the National Birth Defects Prevention Study.
Cogswell ME, Bitsko RH, Anderka M, Caton AR, Feldkamp ML, Hockett Sherlock SM, Meyer RE, Ramadhani T, Robbins JM, Shaw GM, Mathews TJ, Royle M, Reefhuis J; National Birth Defects Prevention Study. Cogswell ME, et al. Among authors: feldkamp ml. Am J Epidemiol. 2009 Oct 15;170(8):975-85. doi: 10.1093/aje/kwp226. Epub 2009 Sep 7. Am J Epidemiol. 2009. PMID: 19736223
AEBP1 gene variants in infants with gastroschisis.
Feldkamp ML, Bowles NE, Botto LD. Feldkamp ML, et al. Birth Defects Res A Clin Mol Teratol. 2012 Sep;94(9):738-42. doi: 10.1002/bdra.23041. Epub 2012 Jul 23. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22821744
124 results