Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia | European Journal of Human Genetics
Ring chromosome 14 complicated with complex partial seizures and hypoplastic corpus callosum - ScienceDirect
Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18 - ScienceDirect
PDF] Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report. | Semantic Scholar
The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients | European Journal of Human Genetics
Ring Chromosome 14 Syndrome - Child Neurology Foundation
Ring chromosome 14 syndrome: MedlinePlus Genetics
Indian Pediatrics - Editorial
Ring 14 | Gene Expression Analysis in Ring Chromosome 14 Syndrome
Ring Chromosome 14 Syndrome
The ring 14 syndrome: Clinical and molecular definition - Zollino - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Ring Chromosome 14 Syndrome - Child Neurology Foundation
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... | Download Scientific Diagram
The ring 14 syndrome - ScienceDirect
Ring chromosome 14 syndrome: MedlinePlus Genetics
Ring Chromosome and Clinical Findings: Reports Cases of 4 Different Chromosomes in Beninese Population
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 14 | Home
PDF] Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report. | Semantic Scholar
Ring Chromosome 14 Syndrome - Child Neurology Foundation
Molecular and clinical characterization of patients with a ring chromosome 11 - ScienceDirect