![Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics - Kristaninta Bangun, Prasetyanugraheni Kreshanti, Vika Tania, Yulia Ariani Aswin, Clara Menna, Leorca Aurino, 2023 Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics - Kristaninta Bangun, Prasetyanugraheni Kreshanti, Vika Tania, Yulia Ariani Aswin, Clara Menna, Leorca Aurino, 2023](https://journals.sagepub.com/cms/10.1177/10556656221149243/asset/images/large/10.1177_10556656221149243-fig2.jpeg)
Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics - Kristaninta Bangun, Prasetyanugraheni Kreshanti, Vika Tania, Yulia Ariani Aswin, Clara Menna, Leorca Aurino, 2023
A karyotype of 46,XY,r(13). The arrows indicate the breakpoints. r(13)... | Download Scientific Diagram
Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. - Document - Gale OneFile: Health and Medicine
![Partial G-banded karyotype of the patient. A. The normal and the ring... | Download Scientific Diagram Partial G-banded karyotype of the patient. A. The normal and the ring... | Download Scientific Diagram](https://www.researchgate.net/publication/282620303/figure/fig1/AS:357676094640128@1462288034447/Partial-G-banded-karyotype-of-the-patient-A-The-normal-and-the-ring-chromosome-13-B.png)
Partial G-banded karyotype of the patient. A. The normal and the ring... | Download Scientific Diagram
![G-banded of the ring chromosome 13 and the normal chromosome 13 on both... | Download Scientific Diagram G-banded of the ring chromosome 13 and the normal chromosome 13 on both... | Download Scientific Diagram](https://www.researchgate.net/publication/256607146/figure/fig2/AS:601695218319376@1520466727740/G-banded-of-the-ring-chromosome-13-and-the-normal-chromosome-13-on-both-patients.png)
G-banded of the ring chromosome 13 and the normal chromosome 13 on both... | Download Scientific Diagram
![Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsj.ejhg.5201194/MediaObjects/41431_2004_Article_BF5201194_Fig1_HTML.jpg)
Refined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics
![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/full/springer-static/image/art%3A10.1038%2Fs41598-021-83399-3/MediaObjects/41598_2021_83399_Fig1_HTML.png)
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming | Scientific Reports
![PDF] Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13. | Semantic Scholar PDF] Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c2aca42a9c9588bb2c8328a9778f425c0f87e450/4-Figure2-1.png)
PDF] Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13. | Semantic Scholar
![PDF) Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: A case report PDF) Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: A case report](https://www.researchgate.net/publication/50374304/figure/fig1/AS:195343976275979@1423585041311/Cytogenetic-cartogram-of-the-case-47-XYY-r13p11q34-The-arrowhead-demonstrates-the_Q320.jpg)
PDF) Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: A case report
![Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature - ScienceDirect Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S102845592030245X-gr1.jpg)
Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature - ScienceDirect
![Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes](https://www.frontiersin.org/files/Articles/613035/fneur-11-613035-HTML/image_m/fneur-11-613035-t001.jpg)
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
![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)
2.5 years boy with ring chromosome 18. 46, XY, r (18) (p11.32 q21.32). | Download Scientific Diagram
![Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13 - Murat Kaya, Ilknur Suer, Tugba Kalayci, Birsen Karaman, Sukru Ozturk, Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13 - Murat Kaya, Ilknur Suer, Tugba Kalayci, Birsen Karaman, Sukru Ozturk,](https://journals.sagepub.com/cms/10.1177/00369330221114426/asset/images/large/10.1177_00369330221114426-fig1.jpeg)
Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13 - Murat Kaya, Ilknur Suer, Tugba Kalayci, Birsen Karaman, Sukru Ozturk,
![Mechanisms of ring chromosome formation, ring instability and clinical consequences | BMC Medical Genetics | Full Text Mechanisms of ring chromosome formation, ring instability and clinical consequences | BMC Medical Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2F1471-2350-12-171/MediaObjects/12881_2011_Article_916_Fig1_HTML.jpg)
Mechanisms of ring chromosome formation, ring instability and clinical consequences | BMC Medical Genetics | Full Text
![PDF] Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches. | Semantic Scholar PDF] Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/89fb30fd468d6648dee685f943165cf6e71f2ee3/4-Figure1-1.png)