Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
Figure 2 from A case with a ring chromosome 22. | Semantic Scholar
![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
Chromosome 22 Ring - Phelan-McDermid Syndrome Foundation
Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text
Amniotic fluid cell culture karyotype showing ring chromosome 22. | Download Scientific Diagram
Chromosome 22: MedlinePlus Genetics
2.5 years boy with ring chromosome 18. 46, XY, r (18) (p11.32 q21.32). | Download Scientific Diagram
Chapter 11 Chromosomes. Cytogenetics Sub-discipline within genetics that links chromosome variations to specific traits, including illnesses. - ppt download
![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
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
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
Ring Chromosome 22 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring Chromosome 22 Syndrome
Ring Chromosome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
Ring 14 Syndrome – Ring14 USA
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![PDF] Prenatal diagnosis of the isodicentric chromosome 22 associated with cat eye syndrome by multiplex ligation-dependent probe amplification | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5fcac29c99711f97345ffdf58fd698b5c077fe3f/2-Figure1-1.png "PDF] Prenatal diagnosis of the isodicentric chromosome 22 associated with cat eye syndrome by multiplex ligation-dependent probe amplification | Semantic Scholar")
PDF] Prenatal diagnosis of the isodicentric chromosome 22 associated with cat eye syndrome by multiplex ligation-dependent probe amplification | Semantic Scholar
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
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 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
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
