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Triple-marker prenatal screening program for chromosomal defects.
Kazerouni NN, Currier B, Malm L, Riggle S, Hodgkinson C, Smith S, Tempelis C, Lorey F, Davis A, Jelliffe-Pawlowski L, Walton-Haynes L, Roberson M. Kazerouni NN, et al. Obstet Gynecol. 2009 Jul;114(1):50-58. doi: 10.1097/AOG.0b013e3181a9479e. Obstet Gynecol. 2009. PMID: 19546758
A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
Wang H, St Julien KR, Stevenson DK, Hoffmann TJ, Witte JS, Lazzeroni LC, Krasnow MA, Quaintance CC, Oehlert JW, Jelliffe-Pawlowski LL, Gould JB, Shaw GM, O'Brodovich HM. Wang H, et al. Pediatrics. 2013 Aug;132(2):290-7. doi: 10.1542/peds.2013-0533. Epub 2013 Jul 29. Pediatrics. 2013. PMID: 23897914 Free PMC article.
Infant C677T MTHFR polymorphism and severe mental retardation.
Shaw GM, Jelliffe-Pawlowski L, Nelson V, Zhu H, Harris JA, Finnell RH. Shaw GM, et al. Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):24-6. doi: 10.1002/bdra.20321. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17149733
164 results