Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome | Journal of Medical Genetics
Frontiers | Case Report: The Emerging Role of Ring Chromosome 22 in Phelan-McDermid Syndrome With Atypical Teratoid/Rhabdoid Tumor: The First Child Treated With Growth Hormone
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... | Download Scientific Diagram
Ring Chromosome 18 Syndrome
Chromosomal abnormalities and IVF: what you need to know
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | Download Scientific Diagram
Ring chromosome 20 syndrome – A rare chromosomal cause of refractory epilepsy in children - ScienceDirect
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) | Journal of Medical Genetics
Ring 22 FTNW
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
Chromosome 22 Ring - Phelan-McDermid Syndrome Foundation
How Are Changes in the Chromosome 22 Related to Health Conditions? - StoryMD
Chromosome 22 - Wikipedia
Ring Chromosome 4 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Karyotype of the described patient. The arrow indicates the ring... | Download Scientific Diagram
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier | Molecular Cytogenetics | Full Text