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Results: 1-8 |
Results: 8
Satellite III sequences on 14p and their relevance to Robertsonian translocation formation
Authors: Bandyopadhyay, R Berend, SA Page, SL Choo, KHA Shaffer, LG
Citation: R. Bandyopadhyay et al., Satellite III sequences on 14p and their relevance to Robertsonian translocation formation, CHROMOS RES, 9(3), 2001, pp. 235-242
Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15
Authors: Abrams, DJ Aronoff, AR Berend, SA Roa, BB Shaffer, LG Geier, MR
Citation: Dj. Abrams et al., Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15, PRENAT DIAG, 21(8), 2001, pp. 676-679
Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derivedfrom chromosome 17: molecular analysis and delineation of the phenotype
Authors: Stankiewicz, P Park, SS Holder, SE Waters, CS Palmer, RW Berend, SA Shaffer, LG Potocki, L Lupski, JR
Citation: P. Stankiewicz et al., Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derivedfrom chromosome 17: molecular analysis and delineation of the phenotype, CLIN GENET, 60(5), 2001, pp. 336-344
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci
Authors: Berend, SA Spikes, AS Kashork, CD Wu, JM Daw, SC Scambler, PJ Shaffer, LG
Citation: Sa. Berend et al., Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci, AM J MED G, 91(4), 2000, pp. 313-317
Deletion (9) (p13.1 p21.1)
Authors: Scaglia, F Bodamer, OAF Berend, SA Adam, LR Shaffer, LG
Citation: F. Scaglia et al., Deletion (9) (p13.1 p21.1), AM J MED G, 91(2), 2000, pp. 113-115
Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes
Authors: Berend, SA Horwitz, J McCaskill, C Shaffer, LG
Citation: Sa. Berend et al., Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes, AM J HU GEN, 66(6), 2000, pp. 1787-1793
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy
Authors: Berend, SA Feldman, GL McCaskill, C Czarnecki, P Van Dyke, DL Shaffer, LG
Citation: Sa. Berend et al., Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy, AM J MED G, 82(3), 1999, pp. 275-281
Pure trisomy 10p involving an isochromosome 10p
Authors: Berend, SA Shaffer, LG Bejjani, BA
Citation: Sa. Berend et al., Pure trisomy 10p involving an isochromosome 10p, CLIN GENET, 55(5), 1999, pp. 367-371
Risultati: 1-8 |