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Detailed molecular analysis of 1p36 in neuroblastoma.
Med Pediatr Oncol. 2001 Jan;36(1):37-41. doi: 10.1002/1096-911X(20010101)36:1<37::AID-MPO1010>3.0.CO;2-L.
Med Pediatr Oncol. 2001.
PMID: 11464901
Loss of heterozygosity for chromosome 14q in neuroblastoma.
Thompson PM, Seifried BA, Kyemba SK, Jensen SJ, Guo C, Maris JM, Brodeur GM, Stram DO, Seeger RC, Gerbing R, Matthay KK, Matise TC, White PS.
Thompson PM, et al. Among authors: seifried ba.
Med Pediatr Oncol. 2001 Jan;36(1):28-31. doi: 10.1002/1096-911X(20010101)36:1<28::AID-MPO1008>3.0.CO;2-0.
Med Pediatr Oncol. 2001.
PMID: 11464899
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Mapping of the kinesin-related gene ATSV to chromosome 2q37.
Keller MP, Seifried BA, Rabin BA, Chance PF.
Keller MP, et al. Among authors: seifried ba.
Hum Genet. 1999 Mar;104(3):254-6. doi: 10.1007/s004390050944.
Hum Genet. 1999.
PMID: 10323250
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Molecular evolution of the CMT1A-REP region: a human- and chimpanzee-specific repeat.
Keller MP, Seifried BA, Chance PF.
Keller MP, et al. Among authors: seifried ba.
Mol Biol Evol. 1999 Aug;16(8):1019-26. doi: 10.1093/oxfordjournals.molbev.a026191.
Mol Biol Evol. 1999.
PMID: 10474898
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Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth disease.
Neumann Y, Toren A, Rechavi G, Seifried B, Shoham NG, Mandel M, Kenet G, Sharon N, Sadeh M, Navon R.
Neumann Y, et al.
Med Pediatr Oncol. 1996 Apr;26(4):280-3. doi: 10.1002/(SICI)1096-911X(199604)26:4<280::AID-MPO12>3.0.CO;2-J.
Med Pediatr Oncol. 1996.
PMID: 8600343
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A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease.
Navon R, Seifried B, Gal-On NS, Sadeh M.
Navon R, et al.
Hum Genet. 1996 May;97(5):685-7. doi: 10.1007/BF02281883.
Hum Genet. 1996.
PMID: 8655153
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