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
De Novo Microdeletion on an Inherited Robertsonian Translocation Chromosome: A Cause for Dysmorphism in the Apparently Balanced
The incidence and type of chromosomal translocations from prenatal diagnosis of 3800 patients in the republic of macedonia. - Abstract - Europe PMC
Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition
De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case
A case of heterologous Robertsonian translocation trisomy 13 with a... | Download Scientific Diagram
Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing - Yip - Translational Pediatrics
Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction - ScienceDirect
Robertsonian translocation in a male child with Down syndrome... | Download Scientific Diagram
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
![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
Parental Origin and Timing of De Novo Robertsonian Translocation Formation: The American Journal of Human Genetics
Bench to Bassinet Pediatric Cardiac Genomics Consortium: CHD GENES
Down Syndrome and Recurrent Abortions Resulting from Robertsonian Translocation 21q21q | Annals of Saudi Medicine
Robertsonian translocation
Induction of site-specific chromosomal translocations in embryonic stem cells by CRISPR/Cas9 | Scientific Reports
Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements | Journal of Medical Genetics
Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing. | Semantic Scholar
![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
Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction - ScienceDirect
A case of mosaic balanced heterologous Robertsonian translocation... | Download Scientific Diagram
Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition
Schematic depiction of UPD formation if there is a maternally inherited... | Download Scientific Diagram
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
