Chromosome 22 - Wikipedia
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
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
Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
Ring Chromosome, williams Syndrome, digeorge Syndrome, chromosome 22, chromosomal Inversion, chromosomal Translocation, genetic Material, gene Duplication, chromosome Abnormality, deletion | Anyrgb
A case with a ring chromosome 22. | Semantic Scholar
How Are Changes in the Chromosome 22 Related to Health Conditions? - StoryMD
Ring chromosome 20 syndrome – A rare chromosomal cause of refractory epilepsy in children - ScienceDirect
Chromosome 22 Ring - Phelan-McDermid Syndrome Foundation
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
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
Ring Chromosome 18 Syndrome
Patient 1 (a, b) at age 2 years and 8 months, and patient 2 (c–e) at... | Download Scientific Diagram
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
![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
Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. - Document - Gale OneFile: Health and Medicine
Ring Chromosome 22 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring Chromosome 4 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | Download Scientific Diagram
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
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
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
