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Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.
Ou Z, Stankiewicz P, Xia Z, Breman AM, Dawson B, Wiszniewska J, Szafranski P, Cooper ML, Rao M, Shao L, South ST, Coleman K, Fernhoff PM, Deray MJ, Rosengren S, Roeder ER, Enciso VB, Chinault AC, Patel A, Kang SH, Shaw CA, Lupski JR, Cheung SW. Ou Z, et al. Among authors: fernhoff pm. Genome Res. 2011 Jan;21(1):33-46. doi: 10.1101/gr.111609.110. Genome Res. 2011. PMID: 21205869 Free PMC article.
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH.
Shchelochkov OA, Li FY, Geraghty MT, Gallagher RC, Van Hove JL, Lichter-Konecki U, Fernhoff PM, Copeland S, Reimschisel T, Cederbaum S, Lee B, Chinault AC, Wong LJ. Shchelochkov OA, et al. Among authors: fernhoff pm. Mol Genet Metab. 2009 Mar;96(3):97-105. doi: 10.1016/j.ymgme.2008.11.167. Epub 2009 Jan 12. Mol Genet Metab. 2009. PMID: 19138872
Heparin cofactor II-thrombin complex: a biomarker of MPS disease.
Randall DR, Colobong KE, Hemmelgarn H, Sinclair GB, Hetty E, Thomas A, Bodamer OA, Volkmar B, Fernhoff PM, Casey R, Chan AK, Mitchell G, Stockler S, Melancon S, Rupar T, Clarke LA. Randall DR, et al. Among authors: fernhoff pm. Mol Genet Metab. 2008 Aug;94(4):456-461. doi: 10.1016/j.ymgme.2008.05.001. Epub 2008 Jun 3. Mol Genet Metab. 2008. PMID: 18511319
Vitamin B12 deficiency in children and adolescents.
Rasmussen SA, Fernhoff PM, Scanlon KS. Rasmussen SA, et al. Among authors: fernhoff pm. J Pediatr. 2001 Jan;138(1):10-7. doi: 10.1067/mpd.2001.112160. J Pediatr. 2001. PMID: 11148506 Review. No abstract available.
Pre- and postnatal diagnosis of trisomy 4 mosaicism.
Marion JP, Fernhoff PM, Korotkin J, Priest JH. Marion JP, et al. Among authors: fernhoff pm. Am J Med Genet. 1990 Nov;37(3):362-5. doi: 10.1002/ajmg.1320370314. Am J Med Genet. 1990. PMID: 2260566
74 results