High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally
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 C, Chern S, Lee C, et al. 2006. 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. Prenat Diagn 26: 138-146.
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, et al. 2006. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs. Prenat Diagn 26: 565-570.
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. 2007. 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. Fetal Diagn Ther 22: 249-253.
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, et al. 1999. 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. Prenat Diagn 19: 1143-1149.
A girl with del(4)(q33) and occipital encephalocele: Clinical description and molecular genetic characterization of a rare patient
Quadrelli R, Strehle EM, Vaglio A, et al. 2007. A girl with del(4)(q33) and occipital encephalocele: clinical description and molecular genetic characterization of a rare patient. Genet Test 11: 4-10.
Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: Two new cases and review of the literature
Ruiz C, Grubs RE, Jewett T, et al. 1996. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature. Am J Med Genet 64: 478-484.