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169 related items for PubMed ID: 8953640
1. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q). Mercier S, Fellmann F, Cattin J, Bresson JL. Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640 [Abstract] [Full Text] [Related]
2. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements. Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W. Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734 [Abstract] [Full Text] [Related]
3. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs. Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L. Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274 [Abstract] [Full Text] [Related]
4. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping. Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R. Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433 [Abstract] [Full Text] [Related]
5. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses. Mechoso B, Vaglio A, Quadrelli A, Mark HF, Huang XL, Milunsky A, Quadrelli R. Fetal Diagn Ther; 2007 Dec; 22(4):249-53. PubMed ID: 17369689 [Abstract] [Full Text] [Related]
6. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ]. Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J. Cas Lek Cesk; 2001 Mar 01; 140(4):122-4. PubMed ID: 11284430 [Abstract] [Full Text] [Related]
7. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization. Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y. Prenat Diagn; 1998 Jul 01; 18(7):725-30. PubMed ID: 9706655 [Abstract] [Full Text] [Related]
8. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NR, Schrock E, Ning Y, Ried T. Prenat Diagn; 1998 Nov 01; 18(11):1174-80. PubMed ID: 9854728 [Abstract] [Full Text] [Related]
9. A complex chromosomal rearrangement associated with Hirschsprung's disease. A case report with a review of the literature. Valioulis I, Aubert D, de Billy B, Bawab F, Karam R. Eur J Pediatr Surg; 2000 Jun 01; 10(3):207-11. PubMed ID: 10982055 [Abstract] [Full Text] [Related]
13. High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally. Quadrelli A, Vaglio A, Quadrelli R, Mechoso B, Fan YS, Huang T. Prenat Diagn; 2007 Oct 01; 27(10):982-3. PubMed ID: 17899566 [No Abstract] [Full Text] [Related]
14. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development. Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S. Eur J Med Genet; 2006 Oct 01; 49(5):431-8. PubMed ID: 16497571 [Abstract] [Full Text] [Related]