Ring chromosome - 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
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Ring Chromosome 22 Syndrome
Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
Figure 2 from A case with a ring chromosome 22. | Semantic Scholar
Chromosome 22: MedlinePlus Genetics
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
![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 Chromosome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring 14 Syndrome – Ring14 USA
Ring Chromosome 22 - Special Needs Resource and Training Blog
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Ring Chromosome 20 – this is what you need to know | Beyond the Ion Channel
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
array cgH results: (a) rearrangement pattern at 22q13: the profile of... | 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
Ring Chromosome 22 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Chromosomal abnormalities and IVF: what you need to know
Karyotype of the described patient. The arrow indicates the ring... | Download Scientific Diagram
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Amniotic fluid cell culture karyotype showing ring chromosome 22. | Download Scientific Diagram
a,B) reconstruction of ring 22 by WgS. (a) coloured arrows indicate... | Download Scientific Diagram
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
