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52 results
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Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15.
Cheung SW, Shaffer LG, Richards CS, Page SL, Riconda DL. Cheung SW, et al. Among authors: page sl. Am J Med Genet. 1997 Oct 3;72(1):47-50. doi: 10.1002/(sici)1096-8628(19971003)72:1<47::aid-ajmg10>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9295074
Parental origin and timing of de novo Robertsonian translocation formation.
Bandyopadhyay R, Heller A, Knox-DuBois C, McCaskill C, Berend SA, Page SL, Shaffer LG. Bandyopadhyay R, et al. Among authors: page sl. Am J Hum Genet. 2002 Dec;71(6):1456-62. doi: 10.1086/344662. Epub 2002 Nov 6. Am J Hum Genet. 2002. PMID: 12424707 Free PMC article. Review.
Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.
Berend SA, Page SL, Atkinson W, McCaskill C, Lamb NE, Sherman SL, Shaffer LG. Berend SA, et al. Among authors: page sl. Am J Hum Genet. 2003 Feb;72(2):488-95. doi: 10.1086/367547. Epub 2002 Dec 23. Am J Hum Genet. 2003. PMID: 12506337 Free PMC article.
Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISH.
Page SL, Earnshaw WC, Choo KH, Shaffer LG. Page SL, et al. Hum Mol Genet. 1995 Feb;4(2):289-94. doi: 10.1093/hmg/4.2.289. Hum Mol Genet. 1995. PMID: 7757082
Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation.
Page SL, Shin JC, Han JY, Choo KH, Shaffer LG. Page SL, et al. Hum Mol Genet. 1996 Sep;5(9):1279-88. doi: 10.1093/hmg/5.9.1279. Hum Mol Genet. 1996. PMID: 8872467
Satellite III sequences on 14p and their relevance to Robertsonian translocation formation.
Bandyopadhyay R, Berend SA, Page SL, Choo KH, Shaffer LG. Bandyopadhyay R, et al. Among authors: page sl. Chromosome Res. 2001;9(3):235-42. doi: 10.1023/a:1016652621226. Chromosome Res. 2001. PMID: 11330398
Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations.
Page SL, Shaffer LG. Page SL, et al. Chromosome Res. 1998 Feb;6(2):115-22. doi: 10.1023/a:1009286929145. Chromosome Res. 1998. PMID: 9543014
Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.
Bandyopadhyay R, McQuillan C, Page SL, Choo KH, Shaffer LG. Bandyopadhyay R, et al. Among authors: page sl. Chromosome Res. 2001;9(3):223-33. doi: 10.1023/a:1016648404388. Chromosome Res. 2001. PMID: 11330397
Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation.
Berend SA, Canún S, McCaskill C, Page SL, Shaffer LG. Berend SA, et al. Among authors: page sl. Am J Med Genet. 1998 Nov 16;80(3):252-9. doi: 10.1002/(sici)1096-8628(19981116)80:3<252::aid-ajmg14>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9843048
Nonhomologous Robertsonian translocations form predominantly during female meiosis.
Page SL, Shaffer LG. Page SL, et al. Nat Genet. 1997 Mar;15(3):231-2. doi: 10.1038/ng0397-231. Nat Genet. 1997. PMID: 9054929 No abstract available.
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