References in Facial Abnormalities in Nablus Mask-Like Facial Syndrome: Multidetector Computed Tomography Findings - Journal of Oral and Maxillofacial Surgery
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype - ScienceDirect
Pashayan syndrome: Blepharonasofacial Malformation
Digital Occlusal Splint for Condylar Reconstruction in Children With Temporomandibular Joint Ankylosis - Journal of Oral and Maxillofacial Surgery
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature - ScienceDirect
Nablus mask‐like facial syndrome: Deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype - Allanson - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature - ScienceDirect
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH | European Journal of Human Genetics
Nablus mask‐like facial syndrome: Deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotype - Allanson - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
Hereditary, Developmental, and Environmental Influences on the Formation of Dentofacial Deformities | Plastic Surgery Key
Figure 2 from The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature. | Semantic Scholar
Kyle O'Reilly named 2019 Chelsea Cohen Courage Award recipient
Nablus mask‐like facial syndrome is caused by a microdeletion of 8q detected by array‐based comparative genomic hybridization - Shieh - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
The O'Reillys - myFace
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome | Genetics in Medicine
Confirmation of Nablus mask-like facial syndrome.
Nablus-mask-like-facial-Syndrom
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature. | Semantic Scholar
Maskengesicht - Wikiwand
Characterization of the ocular findings in the nablus masklike facial syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
PDF) Facial Abnormalities in Nablus Mask-Like Facial Syndrome: Multidetector Computed Tomography Findings
Kyle's Story - myFace
Novel microdeletion syndromes detected by chromosome microarrays | SpringerLink
A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign. - Abstract - Europe PMC
Nablus mask-like facial syndrome - Wikipedia
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature. | Semantic Scholar
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature | Request PDF
Nablus mask‐like facial syndrome is caused by a microdeletion of 8q detected by array‐based comparative genomic hybridization - Shieh - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature | Judith Dagan - Academia.edu
