Kyle O'Reilly named 2019 Chelsea Cohen Courage Award recipient
Facial Abnormalities in Nablus Mask-Like Facial Syndrome: Multidetector Computed Tomography Findings - ScienceDirect
Figure 1 from The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature. | Semantic Scholar
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome
Nablus Mask-Like Facial Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Novel microdeletion syndromes detected by chromosome microarrays | SpringerLink
Le Fort II and Le Fort III Osteotomies for Midface Reconstruction and Considerations for Internal Fixation | SpringerLink
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
Postprocessing in Maxillofacial Multidetector Computed Tomography - Silvio Mazziotti, Alfredo Blandino, Michele Gaeta, Antonio Bottari, Carmelo Sofia, Tommaso D'Angelo, Giorgio Ascenti, 2015
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
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
Characterization of the ocular findings in the nablus masklike facial syndrome - ScienceDirect
PDF) Confirmation of Nablus mask-like facial syndrome | Luciana Rigoli - Academia.edu
Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases | European Journal of Human Genetics
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
A case of Nablus mask-like facial syndrome with autism spect... : Psychiatric Genetics
A framework for the evaluation of patients with congenital facial weakness | Orphanet Journal of Rare Diseases | Full Text
A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype - ScienceDirect
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature - ScienceDirect
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Phenotypic overlap between Blepharo-naso-facial syndrome and Nablus mask-like syndrome. Report from the first Indian family
A familial chromosomal complex rearrangement confirms RUNX1T1 as a causative gene for intellectual disability and suggests that 1p22.1p21.3 duplication is likely benign | Molecular Cytogenetics | Full Text
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 - Jamuar - 2015 -
