A case of heterologous Robertsonian translocation trisomy 13 with a... | Download Scientific Diagram
Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction - ScienceDirect
Biomedicines | Free Full-Text | Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements | Journal of Medical Genetics
The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA | Nature Communications
Parental Origin and Timing of De Novo Robertsonian Translocation Formation: The American Journal of Human Genetics
![PDF] De Novo Robertsonian Translocation t(21; 21) in a Child with Down Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d5e57398d2e1881cd88a1c2329a63de2ef7d28cf/2-Figure2-1.png "PDF] De Novo Robertsonian Translocation t(21; 21) in a Child with Down Syndrome | Semantic Scholar")
PDF] De Novo Robertsonian Translocation t(21; 21) in a Child with Down Syndrome | Semantic Scholar
![PDF] De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c19bfb0137703b90af6052fac32a134cbfeecc7a/2-Figure1-1.png "PDF] De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case | Semantic Scholar")
PDF] De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case | Semantic Scholar
Schematic depiction of UPD formation if there is a maternally inherited... | Download Scientific Diagram
Down Syndrome and Recurrent Abortions Resulting from Robertsonian Translocation 21q21q | Annals of Saudi Medicine
Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report | BMC Pregnancy and Childbirth | Full Text
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver‐Russell patient - Dupont - 2002 - American Journal of Medical Genetics - Wiley Online Library
Bench to Bassinet Pediatric Cardiac Genomics Consortium: CHD GENES
PDF) Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21,+t(15q21q) and 46,XX,-21,+t(21q21q) | Christos S Bartsocas - Academia.edu
Cancers | Free Full-Text | Factors That Affect the Formation of Chromosomal Translocations in Cells
Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing - Yip - Translational Pediatrics
Genes | Free Full-Text | Chromosomal Aberrations in Cattle
Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient | Scientific Reports
Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker ch
Prevalence and Phenotypic Impact of Robertsonian Translocations - FullText - Molecular Syndromology 2021, Vol. 12, No. 1 - Karger Publishers
Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction - ScienceDirect
Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition
Robertsonian translocation in a male child with Down syndrome... | Download Scientific Diagram
![PDF] Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/143867e8eaeec365b9e02fa75fe3cb25935ec655/5-Figure2-1.png "PDF] Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes. | Semantic Scholar")
PDF] Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes. | Semantic Scholar
De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case
Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition
Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10) - ScienceDirect
