Relua ruga Schimb de novo robertsonian translocation marker chromosome Suvenir mușchi reapărea

Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing. | Semantic Scholar

A case of heterologous Robertsonian translocation trisomy 13 with a... | 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

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

Robertsonian translocation in a male child with Down syndrome... | Download Scientific Diagram

PDF) Robertsonian translocation T (21; 21) in a female born to normal parents: a case report | Tulika Nirmolia - Academia.edu

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

Cancers | Free Full-Text | Factors That Affect the Formation of Chromosomal Translocations in Cells

PDF] Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes. | Semantic Scholar

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

Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition

At chromosome level - Genetics - UZ Brussel

De Novo Microdeletion on an Inherited Robertsonian Translocation Chromosome: A Cause for Dysmorphism in the Apparently Balanced

Genes | Free Full-Text | Chromosomal Aberrations in Cattle

PDF] De Novo Robertsonian Translocation t(21; 21) in a Child with Down Syndrome | Semantic Scholar

Robertsonian Translocations - Chromosome Abnormalities and Genetic Counseling , 3rd Edition

Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text

Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction - ScienceDirect

Down Syndrome and Recurrent Abortions Resulting from Robertsonian Translocation 21q21q | Annals of Saudi Medicine

Induction of site-specific chromosomal translocations in embryonic stem cells by CRISPR/Cas9 | Scientific Reports

Robertsonian translocation

Bench to Bassinet Pediatric Cardiac Genomics Consortium: CHD GENES

De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case