Ring 14 Syndrome – Ring14 USA
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 - Wikipedia
Ring Chromosome 20 – this is what you need to know | Beyond the Ion Channel
Ring chromosome 15
Chromosome 22 Ring - Phelan-McDermid Syndrome Foundation
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Chromosomal abnormalities and IVF: what you need to know
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![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
![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2006;11:317-319]](https://www.hkjpaed.org/figure/2006;11;317-319-fig1.jpg "Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2006;11:317-319]")
Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2006;11:317-319]
Ring chromosome 22 - Wikipedia
![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
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
Ring Chromosome 22 Syndrome - DoveMed
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
Mechanisms of ring chromosome formation, ring instability and clinical consequences | BMC Medical Genetics | Full Text
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
Decoding the Ring Chromosome
Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3 - ScienceDirect
Chromosome 22 - Wikipedia
Ring Chromosome 22 - Special Needs Resource and Training Blog
Chapter 11 Chromosomes. Cytogenetics Sub-discipline within genetics that links chromosome variations to specific traits, including illnesses. - ppt download
