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Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies | Molecular Cytogenetics | Full Text
![a) The proband at 20 months. Note the carp-like mouth, hypertelorism,... | Download Scientific Diagram a) The proband at 20 months. Note the carp-like mouth, hypertelorism,... | Download Scientific Diagram](https://www.researchgate.net/profile/Quinn-Stein/publication/23399503/figure/fig1/AS:330552960929806@1455821375485/a-The-proband-at-20-months-Note-the-carp-like-mouth-hypertelorism-and-widely-spaced_Q320.jpg)
a) The proband at 20 months. Note the carp-like mouth, hypertelorism,... | Download Scientific Diagram
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Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report | BMC Medical Genomics | Full Text
![Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies – topic of research paper in Biological sciences. Download scholarly article PDF and read Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies – topic of research paper in Biological sciences. Download scholarly article PDF and read](https://cyberleninka.org/viewer_images/909118/f/1.png)
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies – topic of research paper in Biological sciences. Download scholarly article PDF and read
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Application of Multicolor Banding for Identification of Complex Chromosome 18 Rearrangements - ScienceDirect
Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings. - Document - Gale OneFile: Health and Medicine
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Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects | Molecular Cytogenetics | Full Text
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Identification and Molecular Characterization of a de novo Supernumerary Ring Chromosome 18 in a Patient with Klippel‐Trenaunay Syndrome - Timur - 2004 - Annals of Human Genetics - Wiley Online Library
![Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-021-83399-3/MediaObjects/41598_2021_83399_Fig3_HTML.png)
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype. - Abstract - Europe PMC
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PDF) De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems | Diana Postorivo - Academia.edu
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A case of ring chromosome 18 syndrome treated with a combined orthodontic-prosthodontic approach. | Semantic Scholar
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Blaschkoid hypermelanosis in a patient with ring 18 chromosome - Indian Journal of Dermatology, Venereology and Leprology
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Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature
![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 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](https://jmg.bmj.com/content/jmedgenet/39/4/e17/F1.large.jpg)
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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PDF) Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization
![2.5 years boy with ring chromosome 18. 46, XY, r (18) (p11.32 q21.32). | Download Scientific Diagram 2.5 years boy with ring chromosome 18. 46, XY, r (18) (p11.32 q21.32). | Download Scientific Diagram](https://www.researchgate.net/publication/271592126/figure/fig1/AS:295206403493888@1447394099039/25-years-boy-with-ring-chromosome-18-46-XY-r-18-p1132-q2132.png)