• 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH
• A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype
• A case of Nablus mask-like facial syndrome with autism spectrum disorders
• A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask-like facial syndrome
• Atlantoaxial dislocation in the setting of NMLFS
• Characterization of the ocular findings in the nablus masklike facial syndrome
• Confirmation of Nablus mask-like facial syndrome
• Deletion of chromosome 8q22.1, a critical region for Nablus mask-like facial syndrome: four additional cases support a role of genetic modifiers in the manifestation of the phenotype
• Facial abnormalities in Nablus mask-like facial syndrome: multidetector computed tomography findings
• Intraoral findings of a patient with Nablus mask-like facial syndrome and dental treatment approaches: a case report and literature review
• Nablus mask-like facial syndrome
• Nablus mask-like facial syndrome
• Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization
• Nablus Mask-Like Facial Syndrome with Moderate Developmental Delay
• Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype
• Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion
• Nablus syndrome: Easy to diagnose yet difficult to solve
• Phenotypic overlap between Blepharo-naso-facial syndrome and Nablus mask-like syndrome. Report from the first Indian family
• Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndrome
• The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature
• The Partnership of Medical Genetics and Oral and Maxillofacial Surgery When Evaluating Craniofacial Anomalies