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Page 1
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. Am J Med Genet. 1999 Feb 5;88(1):25-8. Am J Med Genet. 1999. PMID: 10050962 Free PMC article.
Mutations in the Norrie disease gene.
Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181
Mutational analysis of the human MAOA gene.
Tivol EA, Shalish C, Schuback DE, Hsu YP, Breakefield XO. Tivol EA, et al. Among authors: schuback de. Am J Med Genet. 1996 Feb 16;67(1):92-7. doi: 10.1002/(SICI)1096-8628(19960216)67:1<92::AID-AJMG16>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8678123
Analysis of MAOA mutations in humans.
Hsu YP, Schuback DE, Tivol EA, Shalish C, Murphy DL, Breakefield XO. Hsu YP, et al. Among authors: schuback de. Prog Brain Res. 1995;106:67-75. doi: 10.1016/s0079-6123(08)61203-0. Prog Brain Res. 1995. PMID: 8584675 Review. No abstract available.
BanI RFLP at AK1 locus (9q34).
Schuback DE, Ozelius L, Breakefield XO. Schuback DE, et al. 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.
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: schuback de. Genomics. 1992 Nov;14(3):715-20. doi: 10.1016/s0888-7543(05)80173-9. Genomics. 1992. PMID: 1427899 Free article.
RFLP for human DBH (dopamine beta-hydroxylase).
Schuback DE, Ozelius L, Hu G, Craft CM, Raese J, Breakefield XO, Hsu YP. Schuback DE, et al. Nucleic Acids Res. 1990 Jan 25;18(2):387. Nucleic Acids Res. 1990. PMID: 1970168 Free PMC article.
29 results