Nablus mask-like facial syndrome
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
Mike Tindall opens up about George and Charlotte - 9Honey
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
Nablus Mask-Like Facial Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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
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
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
Facial Abnormalities in Nablus Mask-Like Facial Syndrome: Multidetector Computed Tomography Findings - ScienceDirect
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 -
Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases | European Journal of Human Genetics
Le Fort II and Le Fort III Osteotomies for Midface Reconstruction and Considerations for Internal Fixation | SpringerLink
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
Nablus mask-like facial syndrome - Wikipedia
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
Facial Abnormalities in Nablus Mask-Like Facial Syndrome: Multidetector Computed Tomography Findings - ScienceDirect
Oculofacial Manifestations of Chromosomal Aberrations | Ento Key
Novel microdeletion syndromes detected by chromosome microarrays | SpringerLink
Kyle O'Reilly named 2019 Chelsea Cohen Courage Award recipient
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature - ScienceDirect
Characterization of the ocular findings in the nablus masklike facial syndrome
