Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature

Toriello-Carey syndrome with a 6Mb interstitial deletion at 22q12 detected by array CGH

(2011) Edith Said et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Pierre Robin sequence: An institutional experience in the multidisciplinary management of airway, feeding and serous otitis media challenges

(2011) F. Glynn et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Birth incidence and prevalence of tumor-prone syndromes: Estimates from a UK family genetic register service

(2010) D.G. Evans et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Further genotype – phenotype correlations in neurofibromatosis 2

(2009) SK Selvanathan et al.   CLINICAL GENETICS

Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

(2009) Erwin Pauws et al.   HUMAN MOLECULAR GENETICS

Meningioma 1 Is Required for Appropriate Osteoblast Proliferation, Motility, Differentiation, and Function

(2009) Xiaoxue Zhang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Pierre Robin sequence: appearances and 25 years of experience with an innovative treatment protocol

(2009) Kurt-W. Bütow et al.   JOURNAL OF PEDIATRIC SURGERY

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence

(2009) Sabina Benko et al.   NATURE GENETICS

Neurofibromatosis type 2 (NF2): A clinical and molecular review

(2009) D Gareth R Evans   Orphanet Journal of Rare Diseases

The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice

(2008) W. Liu et al.   DEVELOPMENT