PDF] Distinctive Phenotype in a Case of Ring Chromosome 22 with Features of 22q13.3 Deletion Syndrome | Semantic Scholar
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
Ring chromosome 22 - Wikipedia
How Are Changes in the Chromosome 22 Related to Health Conditions? - StoryMD
Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
Ring chromosome 22 - Wikipedia
Patient 1 (a, b) at age 2 years and 8 months, and patient 2 (c–e) at... | Download Scientific Diagram
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
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
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text
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
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
Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... | Download Scientific Diagram
Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. - Document - Gale OneFile: Health and Medicine
Ring Chromosome 18 Syndrome
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | Download Scientific Diagram
Examples of ring chromosome instability using G-banding: A) partial... | Download Scientific Diagram
Chromosome 22 - Wikipedia
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 Chromosome 22 Syndrome
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
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