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Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
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Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
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Ring chromosome 22 and autism: Report and review - MacLean - 2000 - American Journal of Medical Genetics - Wiley Online Library
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Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics
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array cgH results: (a) rearrangement pattern at 22q13: the profile of... | Download Scientific Diagram
![Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-022-00591-4/MediaObjects/13039_2022_591_Fig3_HTML.png)
Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report | Molecular Cytogenetics | Full Text
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a,B) reconstruction of ring 22 by WgS. (a) coloured arrows indicate... | Download Scientific Diagram
![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](https://www.frontiersin.org/files/Articles/741062/fneur-12-741062-HTML/image_m/fneur-12-741062-g004.jpg)
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
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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
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2.5 years boy with ring chromosome 18. 46, XY, r (18) (p11.32 q21.32). | Download Scientific Diagram
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Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
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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
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