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Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, Mueller D, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC. Boyles AL, et al. Among authors: mueller d. Am J Med Genet A. 2006 Dec 15;140(24):2776-85. doi: 10.1002/ajmg.a.31546. Am J Med Genet A. 2006. PMID: 17103432
Practice variation in therapeutic hypothermia for hypoxic ischemic encephalopathy among neonates with congenital heart disease in the United States.
Chawla V, Peluso AM, Ball MK, Tabbutt S, Bailly DK, Mueller D, Rao R, Levy PT; Children’s Hospitals Neonatal Consortium Cardiac Focus Group and the Pediatric Cardiac Critical Care Consortium. Chawla V, et al. Among authors: mueller d. J Perinatol. 2024 Nov 22. doi: 10.1038/s41372-024-02173-1. Online ahead of print. J Perinatol. 2024. PMID: 39578511 No abstract available.
940 results