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A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features.
Dumitrescu CE, Kelly MH, Khosravi A, Hart TC, Brahim J, White KE, Farrow EG, Nathan MH, Murphey MD, Collins MT. Dumitrescu CE, et al. Among authors: farrow eg. Osteoporos Int. 2009 Jul;20(7):1273-8. doi: 10.1007/s00198-008-0775-z. Epub 2008 Nov 4. Osteoporos Int. 2009. PMID: 18982401 Free PMC article.
Recent advances in renal phosphate handling.
Farrow EG, White KE. Farrow EG, et al. Nat Rev Nephrol. 2010 Apr;6(4):207-17. doi: 10.1038/nrneph.2010.17. Epub 2010 Feb 23. Nat Rev Nephrol. 2010. PMID: 20177401 Free PMC article. Review.
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, Russell L, Hinds DA, Hu Y; 23andMe Research Team; Rokas A, Teramo K, Christensen K, Williams SM, Rämet M, Kingsmore SF, Ryckman KK, Hallman M, Muglia LJ. Huusko JM, et al. Among authors: farrow eg. PLoS Genet. 2018 Sep 13;14(9):e1007673. doi: 10.1371/journal.pgen.1007673. eCollection 2018 Sep. PLoS Genet. 2018. PMID: 30212495 Free PMC article.
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.
Farrow EG, Davis SI, Mooney SD, Beighton P, Mascarenhas L, Gutierrez YR, Pitukcheewanont P, White KE. Farrow EG, et al. Am J Med Genet A. 2006 Mar 1;140(5):537-9. doi: 10.1002/ajmg.a.31106. Am J Med Genet A. 2006. PMID: 16470795 No abstract available.
122 results