Ring 18 molecular assessment and clinical consequences

Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism

(2014) Karen E. Hermetz et al.   PLoS Genetics

Establishing a reference group for distal 18q-: clinical description and molecular basis

(2013) Jannine D. Cody et al.   HUMAN GENETICS

Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18

(2013) Ana Spreiz et al.   JOURNAL OF PEDIATRICS

The ring 14 syndrome

(2012) Marcella Zollino et al.   European Journal of Medical Genetics

Disruption of Teashirt Zinc Finger Homeobox 1 Is Associated with Congenital Aural Atresia in Humans

(2011) Ilse Feenstra et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mechanisms of ring chromosome formation, ring instability and clinical consequences

(2011) Roberta S Guilherme et al.   BMC Medical Genetics

The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions

(2011) Minire Hasi et al.   HUMAN GENETICS

Ring chromosome instability evaluation in six patients with autosomal rings

(2010) C.P. Sodr et al.   GENETICS AND MOLECULAR RESEARCH

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

(2010) L. K. Conlin et al.   JOURNAL OF MEDICAL GENETICS

High resolution genomic analysis of 18q− using oligo-microarray comparative genomic hybridization (aCGH)

(2009) Patricia L. Heard et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A