Prenatal Diagnosis of a Fetus with Congenital Heart Defect and Ring Chromosome 14
Molecular and clinical characterization of patients with a ring chromosome 11 - ScienceDirect
PDF] Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report. | Semantic Scholar
Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia | European Journal of Human Genetics
Ring 14 | Home
Ring Chromosome 14 Syndrome - Child Neurology Foundation
Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report
Ring Chromosome 14 Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Nondisjunction and chromosomal anomalies
Ring Chromosome 14 Syndrome
PDF] Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis. | Semantic Scholar
Ring chromosome 14 syndrome: MedlinePlus Genetics
The ring 14 syndrome: Clinical and molecular definition - Zollino - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
Ring Chromosome and Clinical Findings: Reports Cases of 4 Different Chromosomes in Beninese Population
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
▷ Is Ring Chromosome 14 Syndrome hereditary?
PDF] Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report. | Semantic Scholar
Ring chromosome 14 syndrome Chromosome abnormality Genetics, chromosome, angle, text png | PNGEgg
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
Indian Pediatrics - Editorial
Genetic Clinics
Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature
Ring chromosome - Wikipedia
Ring Chromosome 14 Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
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 14 syndrome - Wikipedia
Ring Chromosome 14 Syndrome - Child Neurology Foundation