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Screen for MAOA mutations in target human groups.
Schuback DE, Mulligan EL, Sims KB, Tivol EA, Greenberg BD, Chang SF, Yang SL, Mau YC, Shen CY, Ho MS, Yang NH, Butler MG, Fink S, Schwartz CE, Berlin F, Breakefield XO, Murphy DL, Hsu YP. Schuback DE, et al. Among authors: breakefield xo. Am J Med Genet. 1999 Feb 5;88(1):25-8. Am J Med Genet. 1999. PMID: 10050962 Free PMC article.
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.
Sims KB, Lebo RV, Benson G, Shalish C, Schuback D, Chen ZY, Bruns G, Craig IW, Golbus MS, Breakefield XO. Sims KB, et al. Among authors: breakefield xo. Hum Mol Genet. 1992 May;1(2):83-9. doi: 10.1093/hmg/1.2.83. Hum Mol Genet. 1992. PMID: 1301161
A genetic linkage map of human chromosome 9q.
Ozelius LJ, Kwiatkowski DJ, Schuback DE, Breakefield XO, Wexler NS, Gusella JF, Haines JL. Ozelius LJ, et al. Among authors: breakefield xo. Genomics. 1992 Nov;14(3):715-20. doi: 10.1016/s0888-7543(05)80173-9. Genomics. 1992. PMID: 1427899 Free article.
Linkage analysis in juvenile neuronal ceroid lipofuscinosis.
Haines JL, Yan WL, Boustany RM, Jewell A, Julier C, Breakefield XO, Gusella JF. Haines JL, et al. Among authors: breakefield xo. Am J Med Genet. 1992 Feb 15;42(4):542-5. doi: 10.1002/ajmg.1320420424. Am J Med Genet. 1992. PMID: 1609835
BanI RFLP at AK1 locus (9q34).
Schuback DE, Ozelius L, Breakefield XO. Schuback DE, et al. Among authors: breakefield xo. Nucleic Acids Res. 1991 Oct 25;19(20):5798. doi: 10.1093/nar/19.20.5798-a. Nucleic Acids Res. 1991. PMID: 1682884 Free PMC article. No abstract available.
475 results