https://www.ncbi.nlm.nih.gov/pubmed/26545049/ 

Microdeletion del(22)(q12.1) excluding the MN1 gene in a patient with craniofacial anomalies.

Bosson C, et al. Am J Med Genet A, 2016 Feb. PMID 26545049 

 

https://www.ncbi.nlm.nih.gov/pubmed/25944382/ 

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate.Breckpot J, et al. Eur J Hum Genet, 2016 Jan. PMID 25944382, Free PMC Article

https://www.ncbi.nlm.nih.gov/pubmed/25810350/ 

Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.Beck M, et al. Am J Med Genet A, 2015 May. PMID 25810350

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359208/
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 literatureTom B Davidson, Pedro A Sanchez-Lara, Linda M Randolph, Mark D Krieger, Shi-Qi Wu, Ashok Panigrahy, Hiroyuki Shimada,Anat Erdreich-Epstein

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629907/ 
Mapping of Craniofacial Traits in Outbred Mice Identifies Major Developmental Genes Involved in Shape DeterminationLuisa F. Pallares, Peter Carbonetto, Shyam Gopalakrishnan, Clarissa C. Parker, Cheryl L. Ackert-Bicknell, Abraham A. Palmer, Tautz 

http://www.ashg.org/2009meeting/abstracts/fulltext/f11129.htm 

22q12.1 deletion: a new cause of syndromic mental retardation. A. P. Jinnah, C. Bacino, S. W. Cheung, A. Patel, C. W. Brown

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http://dev.biologists.org/content/develop/135/23/3959.full.pdf?with-ds=yes 
The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice. Wenjin Liu, Yu Lan, Erwin Pauws, Magda A. Meester-Smoor, Philip Stanier, Ellen C. Zwarthoff and Rulang Jiang