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
Karyotype of the described patient. The arrow indicates the ring... | Download Scientific Diagram
Ring Chromosome, williams Syndrome, digeorge Syndrome, chromosome 22, chromosomal Inversion, chromosomal Translocation, genetic Material, gene Duplication, chromosome Abnormality, deletion | Anyrgb
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
Patient 1 (a, b) at age 2 years and 8 months, and patient 2 (c–e) at... | Download Scientific Diagram
Ring Chromosome 18 Syndrome
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) - JMG Contact blog
Ring 22 FTNW
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
What is Phelan-McDermid syndrome? - Phelan-McDermid Syndrome Foundation
Amniotic fluid cell culture karyotype showing ring chromosome 22. | Download Scientific Diagram
Chromosome 22 - Wikipedia
Chromosomal abnormalities and IVF: what you need to know
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
What is Ring Chromosome?- Definition, Mechanism and Abnormalities – KaryotypingHub
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Mosaic Monosomy 22 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... | Download Scientific Diagram
![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
Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
Ideogram and probe strategy to detect the ring 22/del 22 chromosome in... | Download Scientific Diagram
Ring Chromosome 22 Syndrome
