Ring chromosome 20 syndrome – A rare chromosomal cause of refractory epilepsy in children - ScienceDirect
A Comprehensive and Clinical Review of Chromosome 9 Ring Syndrome
Clinical, cytogenetic and molecular study of a case of ring chromosome 10 | Molecular Cytogenetics | Full Text
Clinical features of infertile men carrying a chromosome 9 translocation
Diplotene with ring chromosome (arrow). Fig. 8. Diakinesis with ring... | Download Scientific Diagram
How An Abusive Father Ruined His Son's Life. And What His Daughter Did About It. – ViralNova
Ring Chromosome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring chromosome - Wikipedia
PDF) Ring chromosome 9 in a newborn
Mosaic Ring Chromosome 6 in an Infant with Significant Patent Ductus Arteriosus and Multiple Congenital Anomalies
A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature | Italian Journal of Pediatrics | Full Text
Ring Chromosome 9 Syndrome
Karyotype results containing isodicentric ring chromosome 9 (left) and... | Download Scientific Diagram
Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 - ScienceDirect
Examples of ring chromosome instability using G-banding: A) partial... | Download Scientific Diagram
Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature - ScienceDirect
PDF) Ring chromosome 9 in a dysmorphic child
Karyotype results containing isodicentric ring chromosome 9 (left) and... | Download Scientific Diagram
Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... | Download Scientific Diagram
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
Molecular Cytogenetic Characterization of a Patient Diagnosed with Dimorphic Anemia Carrying De Novo Rare Ring Chromosome 7 alon
Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature | Semantic Scholar
