Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Ring 22 FTNW
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
What is Phelan-McDermid syndrome? - Phelan-McDermid Syndrome Foundation
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
Coexistence of Autism and Ring Chromosome 22
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Chromosome 22 - Wikipedia
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
![PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3d82b1f53d16a00a8ec6f92482d4a73d639cf3e9/2-Figure1-1.png "PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar")
PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
Ring chromosome - Wikipedia
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome | Molecular Cytogenetics | Full Text
ring 22 Archives - Phelan-McDermid Syndrome Foundation
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. - Abstract - Europe PMC
Ring 22 Syndrome | Signs, Symptoms, Support
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
![PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/3d82b1f53d16a00a8ec6f92482d4a73d639cf3e9/2-Figure2-1.png "PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar")
PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
A case of ring chromosome 18 syndrome treated with a combined orthodontic-prosthodontic approach. | Semantic Scholar
The Artistry of Elizabeth Homan: Rare Disease Day
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. - Abstract - Europe PMC
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
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
