• Associated syndromes in patients with Pierre Robin Sequence
• Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?
• Atypical association of Duane retraction syndrome and Bardet Biedl syndrome
• Chromosome 22 marker in a child with Duane syndrome and urogenital abnormalities
• De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder
• De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects
• Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene
• Duane retraction syndrome associated with Rubinstein-Taybi syndrome
• Duane retraction syndrome in a patient with Duchenne muscular dystrophy
• Duane syndrome associated with features of the cat-eye syndrome and mosaicism for a supernumerary chromosome probably derived from number 22
• Duane's retraction syndrome associated with muscular dystrophy
• Duplication 8q12: confirmation of a novel recognizable phenotype with duane retraction syndrome and developmental delay
• Expanding the Phenotype of the <em>FAM149B1</em>-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single Family
• HOXA1 mutations are not a common cause of Mobius syndrome
• Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability
• Multigene deletions on chromosome 20q13.13-q13.2 including SALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay
• Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review
• Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder
• Townes-Brocks Syndrome
• Wildervanck syndrome
• Wildervanck syndrome: an uncommon cause of Duane syndrome