CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Ring chromosome formation and dynamic mosaicism by... | Download Scientific Diagram
Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion - ScienceDirect
Ring chromosome 20 syndrome – A rare chromosomal cause of refractory epilepsy in children - ScienceDirect
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | Download Scientific Diagram
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Ring 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
Phelan-McDermid Syndrome - Child Neurology Foundation
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
Ring chromosome 22 - Wikipedia
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
Ring 22 FTNW
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