Ring chromosome 22 karyotype in a patient with Opitz (BBBG) syndrome - Christodoulou - 1990 - American Journal of Medical Genetics - Wiley Online Library
PDF) Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnormal first trimester screening and choroid plexus cyst detected on … | elif pala - Academia.edu
The Artistry of Elizabeth Homan: Rare Disease Day
What is a chromosome disorder? – YourGenome
A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome | Molecular Cytogenetics | Full Text
What is Phelan-McDermid syndrome? - Phelan-McDermid Syndrome Foundation
Genes | Free Full-Text | Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region. - Abstract - Europe PMC
Chromosome 22 - Wikipedia
Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 Ismail S, Kamel AK, Ashaat EA, Mohamed AM, Zaki MS, Aboul-Ezz EH, Hammad SA, Sayed IS, El
Ring chromosome 22 - Wikipedia
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation | Journal of Medical Genetics
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
CHROMOSOME 22 CENTRAL - Support for disorders of chromosome 22
Ring chromosome - Wikipedia
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | 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
ring 22 Archives - Phelan-McDermid Syndrome Foundation
Figure 2 from Single-nucleotide polymorphism array-based characterization of ring chromosome 18. | Semantic Scholar
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 Syndrome
